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/G | Ancestral: T | Ambiguity code: K | MAF: 0.01 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript, has 2504 individual genotypes and is mentioned in 2 citations.

Variation displays