Original source

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

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

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

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

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