Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.07 (A)
Location

Chromosome 19:42325120 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

19:g.42325120G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays