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
Synonymous variant
Evidence status

Clinical significance

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

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

About this variant

This variant overlaps 16 transcripts, has 1085 sample genotypes and is associated with 2 phenotypes.

Variant displays