SLC22A5 c.951+222C>T

Variant ID: 5-131723065-C-T

NM_003060.3(SLC22A5):c.951+222C>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Evaluation of 71 Coronary Artery Disease Risk Variants in a Multiethnic Cohort.

Frontiers In Cardiovascular Medicine
Ke, Wangjing W; Rand, Kristin A KA; Conti, David V DV; Setiawan, Veronica W VW; Stram, Daniel O DO; Wilkens, Lynne L; Le Marchand, Loic L; Assimes, Themistocles L TL; Haiman, Christopher A CA
Publication Date: 2018

Variant appearance in text: rs17689550
PubMed Link: 29740590
Variant Present in the following documents:
  • Main text
  • fcvm-05-00019.pdf
View BVdb publication page



Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease.

Database : The Journal Of Biological Databases And Curation
Cheema, Asma N AN; Rosenthal, Samantha L SL; Ilyas Kamboh, M M
Publication Date: 2017-01-01

Variant appearance in text: rs17689550
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
  • bax078.pdf
View BVdb publication page



Metabolic heritability at birth: implications for chronic disease research.

Human Genetics
Ryckman, Kelli K KK; Smith, Caitlin J CJ; Jelliffe-Pawlowski, Laura L LL; Momany, Allison M AM; Berberich, Stanton L SL; Murray, Jeffrey C JC
Publication Date: 2014-08

Variant appearance in text: rs17689550
PubMed Link: 24850141
Variant Present in the following documents:
  • Main text
View BVdb publication page



The 5q31 variants associated with psoriasis and Crohn's disease are distinct.

Human Molecular Genetics
Li, Yonghong Y; Chang, Monica M; Schrodi, Steven J SJ; Callis-Duffin, Kristina P KP; Matsunami, Nori N; Civello, Daniel D; Bui, Nam N; Catanese, Joseph J JJ; Leppert, Mark F MF; Krueger, Gerald G GG; Begovich, Ann B AB
Publication Date: 2008-10-01

Variant appearance in text: rs17689550
PubMed Link: 18614543
Variant Present in the following documents:
  • ddn196_1.pdf
View BVdb publication page