Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.02 (-)
Location

Chromosome 1:116908308 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.116908308delG

Variation displays