Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)

Chromosome 12:109800676 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


ClinVar SCV000169072

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 2569 sample genotypes and is associated with 1 phenotype.

Variant displays