Original source

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

Alleles
-/T|MAF: 0.08 (T)
Location

Chromosome 21: between 36460277 and 36460278 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs370968964, rs199889383

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays