Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.47 (A)
Location

Chromosome 21:17414857 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs56823203, rs17833052

HGVS name

21:g.17414857G>A

This variant has assays on 11 chips - click the plus to show

About this variant

This variant has 3761 sample genotypes and is mentioned in 9 citations.

Variant displays