Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.20 (C)
Location

Chromosome 22:51068517 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58699285, rs5770954

HGVS name

22:g.51068517C>G

Variation displays