Original source

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

Alleles
-/TA | MAF: 0.16 (TA)
Location

Chromosome 21: between 43803308 and 43803309 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Variation displays