Original source

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

AA/- | MAF: 0.12 (-)

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