Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 17:27756497 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

17:g.27756497G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

Variant displays