Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.14 (C)
Location

Chromosome 22:33272893 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59895496

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

This variation has assays on 4 chips - click the plus to show

Variation displays