Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W
Location

Chromosome X:154550277 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 26 transcripts.

Variant displays