Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K
Location

Chromosome X:154765465 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM980559

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays