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 | MAF: 0.01 (T)
Location

Chromosome 13:19957232 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.19957232G>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays