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: 0.01 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs61200702

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_Human660W-quad

About this variant

This variant overlaps 1 transcript and has 2552 individual genotypes.

Variation displays