Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.45 (A)

Chromosome X:154046529 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60248475, rs61484111

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 16 transcripts, 1 regulatory feature, has 3864 sample genotypes and is mentioned in 13 citations.

Variant displays