Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 10 chips - click the plus to show

About this variant

This variant has 5808 sample genotypes.

Variant displays