Original source

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

This variant has 4 HGVS names - click the plus to show

About this variant

Variant displays