ZNF512 c.90-5424A>C

Variant ID: 2-27815510-A-C

NM_032434.3(ZNF512):c.90-5424A>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Increased brain volume from higher cereal and lower coffee intake: shared genetic determinants and impacts on cognition and metabolism.

Cerebral Cortex (New York, N.Y. : 1991)
Kang, Jujiao J; Jia, Tianye T; Jiao, Zeyu Z; Shen, Chun C; Xie, Chao C; Cheng, Wei W; Sahakian, Barbara J BJ; Waxman, David D; Feng, Jianfeng J
Publication Date: 2022-11-09

Variant appearance in text: rs13022873
PubMed Link: 35136970
Variant Present in the following documents:
  • supplementary_materials_revised_submit_bhac005.pdf
View BVdb publication page



Systemic Investigation of Promoter-wide Methylome and Genome Variations in Gout.

International Journal Of Molecular Sciences
Tseng, Chia-Chun CC; Wong, Man Chun MC; Liao, Wei-Ting WT; Chen, Chung-Jen CJ; Lee, Su-Chen SC; Yen, Jeng-Hsien JH; Chang, Shun-Jen SJ
Publication Date: 2020-07-01

Variant appearance in text: rs13022873
PubMed Link: 32630231
Variant Present in the following documents:
  • ijms-21-04702-s001.pdf
View BVdb publication page



USAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis.

Genetic Epidemiology
Ray, Debashree D; Pankow, James S JS; Basu, Saonli S
Publication Date: 2016-01

Variant appearance in text: rs13022873
PubMed Link: 26638693
Variant Present in the following documents:
  • Main text
View BVdb publication page



Validated SNPs for eGFR and their associations with albuminuria.

Human Molecular Genetics
Ellis, Jaclyn W JW; Chen, Ming-Huei MH; Foster, Meredith C MC; Liu, Ching-Ti CT; Larson, Martin G MG; de Boer, Ian I; Köttgen, Anna A; Parsa, Afshin A; Bochud, Murielle M; Böger, Carsten A CA; Kao, Linda L; Fox, Caroline S CS; O'Seaghdha, Conall M CM; , ; ,
Publication Date: 2012-07-15

Variant appearance in text: rs13022873
PubMed Link: 22492995
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association for renal traits among participants of African ancestry reveals new loci for renal function.

Plos Genetics
Liu, Ching-Ti CT; Garnaas, Maija K MK; Tin, Adrienne A; Kottgen, Anna A; Franceschini, Nora N; Peralta, Carmen A CA; de Boer, Ian H IH; Lu, Xiaoning X; Atkinson, Elizabeth E; Ding, Jingzhong J; Nalls, Michael M; Shriner, Daniel D; Coresh, Josef J; Kutlar, Abdullah A; Bibbins-Domingo, Kirsten K; Siscovick, David D; Akylbekova, Ermeg E; Wyatt, Sharon S; Astor, Brad B; Mychaleckjy, Josef J; Li, Man M; Reilly, Muredach P MP; Townsend, Raymond R RR; Adeyemo, Adebowale A; Zonderman, Alan B AB; de Andrade, Mariza M; Turner, Stephen T ST; Mosley, Thomas H TH; Harris, Tamara B TB; , ; Rotimi, Charles N CN; Liu, Yongmei Y; Kardia, Sharon L R SL; Evans, Michele K MK; Shlipak, Michael G MG; Kramer, Holly H; Flessner, Michael F MF; Dreisbach, Albert W AW; Goessling, Wolfram W; Cupples, L Adrienne LA; Kao, W Linda WL; Fox, Caroline S CS
Publication Date: 2011-09

Variant appearance in text: rs13022873
PubMed Link: 21931561
Variant Present in the following documents:
  • Main text
  • pgen.1002264.pdf
View BVdb publication page



A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.

Diabetes
Kraja, Aldi T AT; Vaidya, Dhananjay D; Pankow, James S JS; Goodarzi, Mark O MO; Assimes, Themistocles L TL; Kullo, Iftikhar J IJ; Sovio, Ulla U; Mathias, Rasika A RA; Sun, Yan V YV; Franceschini, Nora N; Absher, Devin D; Li, Guo G; Zhang, Qunyuan Q; Feitosa, Mary F MF; Glazer, Nicole L NL; Haritunians, Talin T; Hartikainen, Anna-Liisa AL; Knowles, Joshua W JW; North, Kari E KE; Iribarren, Carlos C; Kral, Brian B; Yanek, Lisa L; O'Reilly, Paul F PF; McCarthy, Mark I MI; Jaquish, Cashell C; Couper, David J DJ; Chakravarti, Aravinda A; Psaty, Bruce M BM; Becker, Lewis C LC; Province, Michael A MA; Boerwinkle, Eric E; Quertermous, Thomas T; Palotie, Leena L; Jarvelin, Marjo-Riitta MR; Becker, Diane M DM; Kardia, Sharon L R SL; Rotter, Jerome I JI; Chen, Yii-Der Ida YD; Borecki, Ingrid B IB
Publication Date: 2011-04

Variant appearance in text: rs13022873
PubMed Link: 21386085
Variant Present in the following documents:
  • Main text
  • 1329.pdf
View BVdb publication page