HMCN1 c.269-20275G>A

Variant ID: 1-185794883-G-A

NM_031935.2(HMCN1):c.269-20275G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.

Annals Of Human Genetics
Jeff, Janina M JM; Ritchie, Marylyn D MD; Denny, Joshua C JC; Kho, Abel N AN; Ramirez, Andrea H AH; Crosslin, David D; Armstrong, Loren L; Basford, Melissa A MA; Wolf, Wendy A WA; Pacheco, Jennifer A JA; Chisholm, Rex L RL; Roden, Dan M DM; Hayes, M Geoffrey MG; Crawford, Dana C DC
Publication Date: 2013-07

Variant appearance in text: rs13375391
PubMed Link: 23534349
Variant Present in the following documents:
  • Main text
View BVdb publication page