Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 20:6766559 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.6766559G>A

Variation displays