CSMD1 c.302+6818A>G

Variant ID: 8-4488046-T-C

NM_033225.5(CSMD1):c.302+6818A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.

Blood
Cooper, Gregory M GM; Johnson, Julie A JA; Langaee, Taimour Y TY; Feng, Hua H; Stanaway, Ian B IB; Schwarz, Ute I UI; Ritchie, Marylyn D MD; Stein, C Michael CM; Roden, Dan M DM; Smith, Joshua D JD; Veenstra, David L DL; Rettie, Allan E AE; Rieder, Mark J MJ
Publication Date: 2008-08-15

Variant appearance in text: rs10503266
PubMed Link: 18535201
Variant Present in the following documents:
  • Main text
View BVdb publication page