Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.02 (T)
Location

Chromosome 1:102876032 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.102876032A>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays