MYH9 c.1013-157C>T

Variant ID: 22-36715837-G-A

NM_002473.4(MYH9):c.1013-157C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


"Replicated" genome wide association for dependence on illegal substances: genomic regions identified by overlapping clusters of nominally positive SNPs.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Drgon, Tomas T; Johnson, Catherine A CA; Nino, Michelle M; Drgonova, Jana J; Walther, Donna M DM; Uhl, George R GR
Publication Date: 2011-03

Variant appearance in text: rs5995281
PubMed Link: 21302341
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

Human Molecular Genetics
Nelson, George W GW; Freedman, Barry I BI; Bowden, Donald W DW; Langefeld, Carl D CD; An, Ping P; Hicks, Pamela J PJ; Bostrom, Meredith A MA; Johnson, Randall C RC; Kopp, Jeffrey B JB; Winkler, Cheryl A CA
Publication Date: 2010-05-01

Variant appearance in text: rs5995281
PubMed Link: 20124285
Variant Present in the following documents:
  • Main text
View BVdb publication page