Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.32 (G)
Location

Chromosome 1:32873002 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58655647

HGVS name

1:g.32873002G>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

Variant displays