Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.21 (A)

Chromosome X:100985100 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs6620968, rs59737572

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 4 transcripts and has 3693 sample genotypes.

Variant displays