Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.04 (G)
Location

Chromosome 10:68987296 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.68987296T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays