Original source

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

Alleles
AA/-|MAF: 0.12 (-)
Location

Chromosome 21:33449342-33449343 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2509 sample genotypes.

Variant displays