Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (T)

Chromosome X:154051703 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61565722

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 16 transcripts, 1 regulatory feature, has 3739 sample genotypes and is mentioned in 2 citations.

Variant displays