F13A1 c.319+17342T>C

Variant ID: 6-6288242-A-G

NM_000129.3(F13A1):c.319+17342T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exploring the interaction between SNP genotype and postmenopausal hormone therapy effects on stroke risk.

Genome Medicine
Huang, Ying Y; Ballinger, Dennis G DG; Stokowski, Renee R; Beilharz, Erica E; Robinson, Jennifer G JG; Liu, Simin S; Robinson, Randal D RD; Henderson, Victor W VW; Rossouw, Jacques E JE; Prentice, Ross L RL
Publication Date: 2012

Variant appearance in text: rs12194855
PubMed Link: 22794791
Variant Present in the following documents:
  • Main text
  • gm358.pdf
View BVdb publication page