Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 1:209788214 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.209788214G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays