Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/C/G | Ancestral: G | Ambiguity code: V | MAF: 0.24 (G)

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 14 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 34 transcripts, has 2182 individual genotypes and is associated with 2 phenotypes.

Variation displays