Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.03 (T)
Location

Chromosome 1:12225374 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.12225374G>T

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays