Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 13:19957198 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.19957198G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays