Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.45 (C)
Location

Chromosome 12:32792173 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_Human610_Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 3119 individual genotypes.

Variation displays