DMD c.6913-372G>A

Variant ID: X-31893862-C-T

NM_004006.2(DMD):c.6913-372G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unrecognized sequence homologies may confound genome-wide association studies.

Nucleic Acids Research
Galichon, Pierre P; Mesnard, Laurent L; Hertig, Alexandre A; Stengel, Bénédicte B; Rondeau, Eric E
Publication Date: 2012-06

Variant appearance in text: rs16989902
PubMed Link: 22362730
Variant Present in the following documents:
  • Main text
  • gks169.pdf
View BVdb publication page