Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.02 (A)
Location

Chromosome 21:34094556 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60995570

This variation has 6 HGVS names - click the plus to show

Variation displays