APOA2 c.100G>C ;(p.V34L)

Variant ID: 1-161192793-C-G

NM_001643.1(APOA2):c.100G>C;(p.V34L)

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: APOA2: Val34Leu
PubMed Link: 22794791
Variant Present in the following documents:
  • Main text
  • gm358.pdf
View BVdb publication page