Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)

Chromosome 14:94769021 (forward strand) | View in location tab


with HGMD-PUBLIC CM0910845

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays