Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.50 (A)

Chromosome X:43678961 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61677452, rs56419047

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3254 sample genotypes and is mentioned in 6 citations.

Variant displays