Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.48 (C)
Location

Chromosome 2:9697372 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36217005

HGVS name

2:g.9697372A>C

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays