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:48524009 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM990496

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and is associated with 2 phenotypes.

Variant displays