Original source

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

-/T | MAF: 0.09 (T)

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

Most severe consequence
Evidence status


Archive dbSNP rs370968964, rs199889383

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

About this variant

This variant overlaps 9 transcripts and has 1093 individual genotypes.

Variation displays