Original source

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

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

Chromosome 3:121568396 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

3:g.121568396A>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2582 sample genotypes.

Variant displays