NR1H3 c.-37-78G>A

Variant ID: 11-47280653-G-A

NM_005693.3(NR1H3):c.-37-78G>A

This variant was identified in 8 publications

View GRCh38 version.




Publications:


PPAR𝛾 Gene and Atherosclerosis: Genetic Polymorphisms, Epigenetics and Therapeutic Implications.

Balkan Journal Of Medical Genetics : Bjmg
Grbić, E E; Peterlin, A A; Kunej, T T; Petrovič, D D
Publication Date: 2018-06

Variant appearance in text: rs12221497
PubMed Link: 30425909
Variant Present in the following documents:
  • Main text
  • bjmg-21-039.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: NR1H3: -37-78G>A; rs12221497
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Nuclear Receptor NR1H3 in Familial Multiple Sclerosis.

Neuron
Wang, Zhe Z; Sadovnick, A Dessa AD; Traboulsee, Anthony L AL; Ross, Jay P JP; Bernales, Cecily Q CQ; Encarnacion, Mary M; Yee, Irene M IM; de Lemos, Madonna M; Greenwood, Talitha T; Lee, Joshua D JD; Wright, Galen G; Ross, Colin J CJ; Zhang, Si S; Song, Weihong W; Vilariño-Güell, Carles C
Publication Date: 2016-06-01

Variant appearance in text: rs12221497
PubMed Link: 27253448
Variant Present in the following documents:
  • Main text
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs12221497
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
View BVdb publication page



Liver X receptors alpha gene (NR1H3) promoter polymorphisms are associated with systemic lupus erythematosus in Koreans.

Arthritis Research & Therapy
Jeon, Ja-Young JY; Nam, Jin-Young JY; Kim, Hyoun-Ah HA; Park, Yong-Beom YB; Bae, Sang-Cheol SC; Suh, Chang-Hee CH
Publication Date: 2014-05-14

Variant appearance in text: rs12221497
PubMed Link: 24886807
Variant Present in the following documents:
  • Main text
  • ar4563.pdf
View BVdb publication page



The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population.

Plos One
Alobeidy, Barrak F BF; Li, Cong C; Alzobair, Alya A AA; Liu, Tao T; Zhao, Junzhang J; Fang, Yuan Y; Zheng, Fang F
Publication Date: 2013

Variant appearance in text: rs12221497
PubMed Link: 23840567
Variant Present in the following documents:
  • Main text
  • pone.0066976.pdf
View BVdb publication page



Liver X receptor α gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study.

Pharmacogenetics And Genomics
Price, Elvin Tyrone ET; Pacanowski, Michael A MA; Martin, Michael A MA; Cooper-DeHoff, Rhonda M RM; Pepine, Carl J CJ; Zineh, Issam I; Johnson, Julie A JA
Publication Date: 2011-06

Variant appearance in text: rs12221497
PubMed Link: 21562465
Variant Present in the following documents:
  • Main text
View BVdb publication page



Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort study.

Bmc Medical Genetics
Dahlman, Ingrid I; Nilsson, Maria M; Gu, Harvest F HF; Lecoeur, Cecile C; Efendic, Suad S; Ostenson, Claes G CG; Brismar, Kerstin K; Gustafsson, Jan-Ake JA; Froguel, Philippe P; Vaxillaire, Martine M; Dahlman-Wright, Karin K; Steffensen, Knut R KR
Publication Date: 2009-03-17

Variant appearance in text: rs12221497
PubMed Link: 19292929
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-27.pdf
View BVdb publication page