Original source

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

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

Chromosome 21:45512414 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61437544, rs3190718

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 3763 sample genotypes and is mentioned in 3 citations.

Variant displays