MYL2 c.169+358T>C

Variant ID: 12-111353161-A-G

NM_000432.3(MYL2):c.169+358T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


cgaTOH: extended approach for identifying tracts of homozygosity.

Plos One
Zhang, Li L; Orloff, Mohammed S MS; Reber, Sean S; Li, Shengchao S; Zhao, Ye Y; Eng, Charis C
Publication Date: 2013

Variant appearance in text: rs17192160
PubMed Link: 23469237
Variant Present in the following documents:
  • Main text
  • pone.0057772.pdf
View BVdb publication page