Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.40 (A)

Chromosome 19:45306777 (forward strand) | View in location tab


with COSMIC COSM3766376 (A/G)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 5 transcripts, has 4368 sample genotypes and is mentioned in 2 citations.

Variant displays