Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.06 (A)
Location

Chromosome 2:119605760 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.119605760A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays