Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome X:19355713 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM920573, CM084910

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 7528, 25917

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and is associated with 2 phenotypes.

Variant displays