Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (C)
Location

Chromosome 19:33386607 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.33386607T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays