Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.48 (G)

Chromosome 19:15184323 (forward strand) | View in location tab


with COSMIC COSM4131311 (G/A), COSM4131312 (G/A)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs57387743

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3817 sample genotypes and is mentioned in 3 citations.

Variant displays