Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.36 (G)
Location

Chromosome 12:52707610 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.52707610A>G

Genotyping chips

This variation has assays on: Illumina_Human660W-quad

Variation displays