Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)

Chromosome 13:46895805 (forward strand) | View in location tab


with COSMIC COSM3753711 (G/A) ; HGMD-PUBLIC CM960851

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4438 sample genotypes and is mentioned in 99 citations.

Variant displays