Original source

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

Alleles
C/A|Ancestral: A|Ambiguity code: M|MAF: 0.45 (C)
Location

Chromosome 1:63708082 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs59888296

HGVS name

1:g.63708082C>A

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant has 5808 sample genotypes.

Variant displays