Original source

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

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

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


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

Most severe consequence
Evidence status

Clinical significance

This variation has 7 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 17 transcripts, has 1085 individual genotypes and is associated with 1 phenotype.

Variation displays