Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.49 (C)
Location

Chromosome 20:22032876 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs582426, rs57456154

HGVS name

20:g.22032876C>T

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant has 3688 sample genotypes and is mentioned in 2 citations.

Variant displays