Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.29 (A)
Location

Chromosome 9:132426231 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.132426231A>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays