Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.19 (G)
Location

Chromosome 22:41992837 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57675069, rs9623488

This variation has 5 HGVS names - click the plus to show

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

Variation displays