Original source

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

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

Chromosome X:31178751 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_078_DMD_300377_0067, 7182

HGVS names

This variant has 35 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and is associated with 3 phenotypes.

Variant displays