Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 4:73740265 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

4:g.73740265A>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

Variant displays