This variation maps to 2 locations

Select a location:
Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.42 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs58682076

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni2.5

About this variant

This variant overlaps 1 transcript and has 2507 individual genotypes.

Variation displays