Original source

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

A/G/T|Ambiguity code: D

Chromosome X:38352697 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM971091, CM062983

Most severe consequence
Start lost
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays