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: 0.46 (A)
Location

Chromosome 21:17414857 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56823203, rs17833052

HGVS name

21:g.17414857G>A

This variation has assays on 10 chips - click the plus to show

Variation displays