Original source

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

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

Chromosome 10:111076234 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.111076234G>T

Genotyping chips

This variation has assays on: Illumina_Human610_Quad, Illumina_1M-duo

Variation displays