Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.40 (G)
Location

Chromosome 7:128468533 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60616659, rs3807130

HGVS name

7:g.128468533A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays