Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.42 (-)
Location

Chromosome 5:132868756 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

5:g.132868756delG

Variation displays