Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.22 (G)

Chromosome X:100987316 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs6620969, rs59954872

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 4 transcripts and has 3689 sample genotypes.

Variant displays