Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

Chromosome X:32501833 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930192 ; PhenCode DMD:c.2302C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 26261

This variation has 25 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and is associated with 1 phenotype.

Variation displays