Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
-/T | MAF: 0.09 (T)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs370968964, rs199889383

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

Variation displays