DMD c.5922+14651A>C

Variant ID: X-32345566-T-G

NM_004006.2(DMD):c.5922+14651A>C

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:

A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts.

Plos One
Skare, Øivind Ø; Gjessing, Håkon K HK; Gjerdevik, Miriam M; Haaland, Øystein A ØA; Romanowska, Julia J; Lie, Rolv T RT; Jugessur, Astanand A
Publication Date: 2017

Variant appearance in text: rs3788899
PubMed Link: 28877219
Variant Present in the following documents:
  • Main text
  • pone.0183772.pdf
View BVdb publication page