Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 20:938920 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.938920C>G

Variation displays