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: 0.11 (C)
Location

Chromosome 22:50581640 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs5770787

This variation has 11 HGVS names - click the plus to show

Variation displays