Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 20:21872462 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs58361976

HGVS name

20:g.21872462C>T

This variant has assays on 14 chips - click the plus to show

About this variant

This variant has 3971 sample genotypes, is associated with 2 phenotypes and is mentioned in 5 citations.

Variant displays