Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.14 (A)
Location

Chromosome 21:26055940 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61531601, rs17585692

This variation has 12 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays