Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.14 (A)
Location

Chromosome 12:72332153 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR073562

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56853432

HGVS name

12:g.72332153T>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays