Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.47 (A)
Location

Chromosome 21:45512414 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61437544, rs3190718

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

This variation has assays on 6 chips - click the plus to show

Variation displays