Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.02 (A)
Location

Chromosome 20:46709416 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.46709416C>A

Variation displays