Original source

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

C/A/G | Ancestral: G | Ambiguity code: V | MAF: 0.43 (C)

Chromosome 12:132676210 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs56856859

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts and has 2929 sample genotypes.

Variant displays