SLC39A8 c.841-8846T>C

Variant ID: 4-103198082-A-G

NM_001135146.1(SLC39A8):c.841-8846T>C

This variant was identified in 24 publications

View GRCh38 version.




Publications:


Multi-trait genome-wide association analyses leveraging alcohol use disorder findings identify novel loci for smoking behaviors in the Million Veteran Program.

Translational Psychiatry
Cheng, Youshu Y; Dao, Cecilia C; Zhou, Hang H; Li, Boyang B; Kember, Rachel L RL; Toikumo, Sylvanus S; Zhao, Hongyu H; Gelernter, Joel J; Kranzler, Henry R HR; Justice, Amy C AC; Xu, Ke K
Publication Date: 2023-05-05

Variant appearance in text: rs13135092
PubMed Link: 37147289
Variant Present in the following documents:
  • Main text
  • 41398_2023_Article_2409.pdf
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Visceral adipose tissue and risk of COVID-19 susceptibility, hospitalization, and severity: A Mendelian randomization study.

Frontiers In Public Health
Chen, Lu L; Sun, Xingang X; Han, Deheng D; Zhong, Jiawei J; Zhang, Han H; Zheng, Liangrong L
Publication Date: 2022

Variant appearance in text: rs13135092
PubMed Link: 36339142
Variant Present in the following documents:
  • Main text
  • fpubh-10-1023935.pdf
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Genomic Predictors of Brisk Walking Are Associated with Elite Sprinter Status.

Genes
Guilherme, João Paulo L F JPLF; Semenova, Ekaterina A EA; Larin, Andrey K AK; Yusupov, Rinat A RA; Generozov, Edward V EV; Ahmetov, Ildus I II
Publication Date: 2022-09-23

Variant appearance in text: rs13135092
PubMed Link: 36292594
Variant Present in the following documents:
  • Main text
  • genes-13-01710.pdf
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Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk.

Translational Psychiatry
Barr, Peter B PB; Mallard, Travis T TT; Sanchez-Roige, Sandra S; Poore, Holly E HE; Linnér, Richard Karlsson RK; , ; Waldman, Irwin D ID; Palmer, Abraham A AA; Harden, K Paige KP; Dick, Danielle M DM
Publication Date: 2022-09-30

Variant appearance in text: rs13135092
PubMed Link: 36180423
Variant Present in the following documents:
  • Main text
  • 41398_2022_Article_2171.pdf
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Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci.

Molecular Psychiatry
Deak, Joseph D JD; Zhou, Hang H; Galimberti, Marco M; Levey, Daniel F DF; Wendt, Frank R FR; Sanchez-Roige, Sandra S; Hatoum, Alexander S AS; Johnson, Emma C EC; Nunez, Yaira Z YZ; Demontis, Ditte D; Børglum, Anders D AD; Rajagopal, Veera M VM; Jennings, Mariela V MV; Kember, Rachel L RL; Justice, Amy C AC; Edenberg, Howard J HJ; Agrawal, Arpana A; Polimanti, Renato R; Kranzler, Henry R HR; Gelernter, Joel J
Publication Date: 2022-10

Variant appearance in text: rs13135092
PubMed Link: 35879402
Variant Present in the following documents:
  • Main text
  • 41380_2022_Article_1709.pdf
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Genetics and sports performance: the present and future in the identification of talent for sports based on DNA testing.

European Journal Of Applied Physiology
Varillas-Delgado, David D; Del Coso, Juan J; Gutiérrez-Hellín, Jorge J; Aguilar-Navarro, Millán M; Muñoz, Alejandro A; Maestro, Antonio A; Morencos, Esther E
Publication Date: 2022-08

Variant appearance in text: rs13135092
PubMed Link: 35428907
Variant Present in the following documents:
  • Main text
  • 421_2022_Article_4945.pdf
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Genes and Weightlifting Performance.

Genes
Kikuchi, Naoki N; Moreland, Ethan E; Homma, Hiroki H; Semenova, Ekaterina A EA; Saito, Mika M; Larin, Andrey K AK; Kobatake, Naoyuki N; Yusupov, Rinat A RA; Okamoto, Takanobu T; Nakazato, Koichi K; Williams, Alun G AG; Generozov, Edward V EV; Ahmetov, Ildus I II
Publication Date: 2021-12-23

Variant appearance in text: rs13135092
PubMed Link: 35052366
Variant Present in the following documents:
  • Main text
  • genes-13-00025.pdf
View BVdb publication page



Genes and Weightlifting Performance.

Genes
Kikuchi, Naoki N; Moreland, Ethan E; Homma, Hiroki H; Semenova, Ekaterina A EA; Saito, Mika M; Larin, Andrey K AK; Kobatake, Naoyuki N; Yusupov, Rinat A RA; Okamoto, Takanobu T; Nakazato, Koichi K; Williams, Alun G AG; Generozov, Edward V EV; Ahmetov, Ildus I II
Publication Date: 2021-12-23

Variant appearance in text: rs13135092
PubMed Link: 35052366
Variant Present in the following documents:
  • Main text
  • genes-13-00025.pdf
View BVdb publication page



FAAH and CNR1 Polymorphisms in the Endocannabinoid System and Alcohol-Related Sleep Quality.

Frontiers In Psychiatry
Soundararajan, Soundarya S; Kazmi, Narjis N; Brooks, Alyssa T AT; Krumlauf, Michael M; Schwandt, Melanie L ML; George, David T DT; Hodgkinson, Colin A CA; Wallen, Gwenyth R GR; Ramchandani, Vijay A VA
Publication Date: 2021

Variant appearance in text: rs13135092
PubMed Link: 34566715
Variant Present in the following documents:
  • Main text
  • fpsyt-12-712178.pdf
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Genetically Predicted Insomnia in Relation to 14 Cardiovascular Conditions and 17 Cardiometabolic Risk Factors: A Mendelian Randomization Study.

Journal Of The American Heart Association
Liu, Xinhui X; Li, Chuanbao C; Sun, Xiaoru X; Yu, Yuanyuan Y; Si, Shucheng S; Hou, Lei L; Yan, Ran R; Yu, Yifan Y; Li, Mingzhuo M; Li, Hongkai H; Xue, Fuzhong F
Publication Date: 2021-08-03

Variant appearance in text: rs13135092
PubMed Link: 34315237
Variant Present in the following documents:
  • JAH3-10-e020187.pdf
  • JAH3-10-e020187-s001.pdf
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Causal effect of alcohol use on the risk of end-stage kidney disease and related comorbidities: a Mendelian randomization study.

Kidney Research And Clinical Practice
Park, Sehoon S; Lee, Soojin S; Kim, Yaerim Y; Lee, Yeonhee Y; Kang, Min Woo MW; Kim, Kwangsoo K; Kim, Yong Chul YC; Han, Seung Seok SS; Lee, Hajeong H; Lee, Jung Pyo JP; Joo, Kwon Wook KW; Lim, Chun Soo CS; Kim, Yon Su YS; Kim, Dong Ki DK
Publication Date: 2021-06

Variant appearance in text: rs13135092
PubMed Link: 34024088
Variant Present in the following documents:
  • Main text
  • j-krcp-20-186.pdf
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Genetics of substance use disorders: a review.

Psychological Medicine
Deak, Joseph D JD; Johnson, Emma C EC
Publication Date: 2021-10

Variant appearance in text: rs13135092
PubMed Link: 33879270
Variant Present in the following documents:
  • Main text
View BVdb publication page



Brain Magnetic Resonance Imaging Phenome-Wide Association Study With Metal Transporter Gene SLC39A8.

Frontiers In Genetics
Hermann, Evan R ER; Chambers, Emily E; Davis, Danielle N DN; Montgomery, McKale R MR; Lin, Dingbo D; Chowanadisai, Winyoo W
Publication Date: 2021

Variant appearance in text: rs13135092
PubMed Link: 33790950
Variant Present in the following documents:
  • Main text
  • fgene-12-647946.pdf
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Genetics of 35 blood and urine biomarkers in the UK Biobank.

Nature Genetics
Sinnott-Armstrong, Nasa N; Tanigawa, Yosuke Y; Amar, David D; Mars, Nina N; Benner, Christian C; Aguirre, Matthew M; Venkataraman, Guhan Ram GR; Wainberg, Michael M; Ollila, Hanna M HM; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Pirruccello, James P JP; Qian, Junyang J; Shcherbina, Anna A; , ; Rodriguez, Fatima F; Assimes, Themistocles L TL; Agarwala, Vineeta V; Tibshirani, Robert R; Hastie, Trevor T; Ripatti, Samuli S; Pritchard, Jonathan K JK; Daly, Mark J MJ; Rivas, Manuel A MA
Publication Date: 2021-02

Variant appearance in text: SLC39A8: 841-8846T>C; rs13135092
PubMed Link: 33462484
Variant Present in the following documents:
  • NIHMS1651539-supplement-2.xlsx, sheet 21
View BVdb publication page



Genetics of pain: From rare Mendelian disorders to genetic predisposition to pain.

Acta Bio-Medica : Atenei Parmensis
Naureen, Zakira Z; Lorusso, Lorenzo L; Manganotti, Paolo P; Caruso, Paola P; Mazzon, Giulia G; Cecchin, Stefano S; Marceddu, Giuseppe G; Bertelli, Matteo M
Publication Date: 2020-11-09

Variant appearance in text: rs13135092
PubMed Link: 33170156
Variant Present in the following documents:
  • Main text
  • ACTA-91-10.pdf
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Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs13135092
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions.

Communications Biology
Tsepilov, Yakov A YA; Freidin, Maxim B MB; Shadrina, Alexandra S AS; Sharapov, Sodbo Z SZ; Elgaeva, Elizaveta E EE; Zundert, Jan van JV; Karssen, Lennart С LС; Suri, Pradeep P; Williams, Frances M K FMK; Aulchenko, Yurii S YS
Publication Date: 2020-06-25

Variant appearance in text: rs13135092
PubMed Link: 32587327
Variant Present in the following documents:
  • Main text
View BVdb publication page



Using polygenic scores for identifying individuals at increased risk of substance use disorders in clinical and population samples.

Translational Psychiatry
Barr, Peter B PB; Ksinan, Albert A; Su, Jinni J; Johnson, Emma C EC; Meyers, Jacquelyn L JL; Wetherill, Leah L; Latvala, Antti A; Aliev, Fazil F; Chan, Grace G; Kuperman, Samuel S; Nurnberger, John J; Kamarajan, Chella C; Anokhin, Andrey A; Agrawal, Arpana A; Rose, Richard J RJ; Edenberg, Howard J HJ; Schuckit, Marc M; Kaprio, Jaakko J; Dick, Danielle M DM
Publication Date: 2020-06-18

Variant appearance in text: rs13135092
PubMed Link: 32555147
Variant Present in the following documents:
  • 41398_2020_865_MOESM1_ESM.pdf
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Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits.

Nature Neuroscience
Zhou, Hang H; Sealock, Julia M JM; Sanchez-Roige, Sandra S; Clarke, Toni-Kim TK; Levey, Daniel F DF; Cheng, Zhongshan Z; Li, Boyang B; Polimanti, Renato R; Kember, Rachel L RL; Smith, Rachel Vickers RV; Thygesen, Johan H JH; Morgan, Marsha Y MY; Atkinson, Stephen R SR; Thursz, Mark R MR; Nyegaard, Mette M; Mattheisen, Manuel M; Børglum, Anders D AD; Johnson, Emma C EC; Justice, Amy C AC; Palmer, Abraham A AA; McQuillin, Andrew A; Davis, Lea K LK; Edenberg, Howard J HJ; Agrawal, Arpana A; Kranzler, Henry R HR; Gelernter, Joel J
Publication Date: 2020-07

Variant appearance in text: rs13135092
PubMed Link: 32451486
Variant Present in the following documents:
  • Main text
  • nihms-1585622.pdf
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Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes.

Nature Communications
Wang, Heming H; Lane, Jacqueline M JM; Jones, Samuel E SE; Dashti, Hassan S HS; Ollila, Hanna M HM; Wood, Andrew R AR; van Hees, Vincent T VT; Brumpton, Ben B; Winsvold, Bendik S BS; Kantojärvi, Katri K; Palviainen, Teemu T; Cade, Brian E BE; Sofer, Tamar T; Song, Yanwei Y; Patel, Krunal K; Anderson, Simon G SG; Bechtold, David A DA; Bowden, Jack J; Emsley, Richard R; Kyle, Simon D SD; Little, Max A MA; Loudon, Andrew S AS; Scheer, Frank A J L FAJL; Purcell, Shaun M SM; Richmond, Rebecca C RC; Spiegelhalder, Kai K; Tyrrell, Jessica J; Zhu, Xiaofeng X; Hublin, Christer C; Kaprio, Jaakko A JA; Kristiansson, Kati K; Sulkava, Sonja S; Paunio, Tiina T; Hveem, Kristian K; Nielsen, Jonas B JB; Willer, Cristen J CJ; Zwart, John-Anker JA; Strand, Linn B LB; Frayling, Timothy M TM; Ray, David D; Lawlor, Deborah A DA; Rutter, Martin K MK; Weedon, Michael N MN; Redline, Susan S; Saxena, Richa R
Publication Date: 2019-08-13

Variant appearance in text: rs13135092
PubMed Link: 31409809
Variant Present in the following documents:
  • Main text
  • 41467_2019_11456_MOESM10_ESM.pdf
  • 41467_2019_Article_11456.pdf
View BVdb publication page



Genome-wide association study of multisite chronic pain in UK Biobank.

Plos Genetics
Johnston, Keira J A KJA; Adams, Mark J MJ; Nicholl, Barbara I BI; Ward, Joey J; Strawbridge, Rona J RJ; Ferguson, Amy A; McIntosh, Andrew M AM; Bailey, Mark E S MES; Smith, Daniel J DJ
Publication Date: 2019-06

Variant appearance in text: rs13135092
PubMed Link: 31194737
Variant Present in the following documents:
  • Main text
  • pgen.1008164.pdf
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Genetic architecture of human thinness compared to severe obesity.

Plos Genetics
Riveros-McKay, Fernando F; Mistry, Vanisha V; Bounds, Rebecca R; Hendricks, Audrey A; Keogh, Julia M JM; Thomas, Hannah H; Henning, Elana E; Corbin, Laura J LJ; , ; O'Rahilly, Stephen S; Zeggini, Eleftheria E; Wheeler, Eleanor E; Barroso, Inês I; Farooqi, I Sadaf IS
Publication Date: 2019-01

Variant appearance in text: rs13135092
PubMed Link: 30677029
Variant Present in the following documents:
  • Main text
  • pgen.1007603.pdf
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Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts.

The American Journal Of Psychiatry
Sanchez-Roige, Sandra S; Palmer, Abraham A AA; Fontanillas, Pierre P; Elson, Sarah L SL; , ; Adams, Mark J MJ; Howard, David M DM; Edenberg, Howard J HJ; Davies, Gail G; Crist, Richard C RC; Deary, Ian J IJ; McIntosh, Andrew M AM; Clarke, Toni-Kim TK
Publication Date: 2019-02-01

Variant appearance in text: rs13135092
PubMed Link: 30336701
Variant Present in the following documents:
  • Main text
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Detection and interpretation of shared genetic influences on 42 human traits.

Nature Genetics
Pickrell, Joseph K JK; Berisa, Tomaz T; Liu, Jimmy Z JZ; Ségurel, Laure L; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-07

Variant appearance in text: rs13135092
PubMed Link: 27182965
Variant Present in the following documents:
  • NIHMS780506-supplement-5.pdf
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Genome-wide association analysis implicates elastic microfibrils in the development of nonsyndromic striae distensae.

The Journal Of Investigative Dermatology
Tung, Joyce Y JY; Kiefer, Amy K AK; Mullins, Meghan M; Francke, Uta U; Eriksson, Nicholas N
Publication Date: 2013-11

Variant appearance in text: rs13135092
PubMed Link: 23633020
Variant Present in the following documents:
  • jid2013196x1.pdf
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