Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.06 (A)

Chromosome X:19343950 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status


Archive dbSNP rs7059385

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 9 transcripts and has 2924 sample genotypes.

Variant displays