Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: < 0.01 (T)
Location

Chromosome 17:40309098 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.40309098G>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

Variant displays