Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome X:83509032 (forward strand) | View in location tab


with COSMIC COSM4157035 (A/G), COSM4157034 (A/G)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs58335216

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 2893 sample genotypes and is associated with 1 phenotype.

Variant displays