Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R

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


with COSMIC COSM4157035 (A/G), COSM4157034 (A/G) ; dbSNP rs111919890 (-/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs58335216

This variant has 3 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 389 sample genotypes and is associated with 1 phenotype.

Variant displays