Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.37 (A)

Chromosome 13:27665833 (forward strand) | View in location tab


with COSMIC COSM147656 (G/A)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

Variant displays