Original source

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

Alleles
-/A | MAF: 0.01 (A)
Location

Chromosome 21: between 36460365 and 36460366 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs375838101

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

About this variant

Variant displays