Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A|Ancestral: G|Ambiguity code: R

Chromosome X:31177932 (forward strand)|View in location tab

Co-located variants
Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 2010_April_001_080_DMD_300377_0070, 7185

HGVS names

This variant has 29 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and is associated with 2 phenotypes.

Variant displays