Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.40 (A)
Location

Chromosome 12:52674706 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61490963

HGVS name

12:g.52674706T>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays