Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.46 (G)

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


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

Most severe consequence
Evidence status


Archive dbSNP rs57387743

This variation has 3 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2413 individual genotypes and is mentioned in 3 citations.

Variation displays