Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.06 (A)
Location

Chromosome 15:89345296 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

15:g.89345296G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays