Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.11 (T)
Location

Chromosome 10:112835992 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.112835992G>T

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_Human610_Quad

Variation displays