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DMD c.8391-3870G>T
Variant ID: X-31518931-C-A
NM_004006.2(
DMD
):c.8391-3870G>T
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: rs16989676
PubMed Link:
22362730
Variant Present in the following documents:
Main text
gks169.pdf
View BVdb publication page