Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.40 (A)
Location

Chromosome 1:75126480 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

1:g.75126480G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2852 sample genotypes.

Variant displays