Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.48 (A)
Location

Chromosome 2:119599735 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58503071

HGVS name

2:g.119599735A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays