Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 17:64319272 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

17:g.64319272C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

Variant displays