Original source

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

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

Chromosome X:48528351 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM002590, CM024395

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 6922, 2010_April_001_088_EBP_300205_0011

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays