Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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