Original source

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

A/C/G | Ancestral: G | Ambiguity code: V | MAF: 0.30 (G)

Chromosome X:19355721 (forward strand) | View in location tab


with COSMIC COSM3759444 (A/G), COSM3759442 (A/G), COSM3759443 (A/G)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 32 transcripts, has 3589 sample genotypes and is associated with 1 phenotype.

Variant displays