Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:48917403 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

8:g.48917403G>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays