Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 22:37196448 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.37196448T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays