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
Location

Chromosome 7:101126565 (forward strand) | View in location tab

Most severe consequence
HGVS name

7:g.101126565T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays