Original source

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

-/T | MAF: 0.08 (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 2505 individual genotypes.

Variation displays