Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.25 (C)
Location

Chromosome 19:5830431 (forward strand) | View in location tab

Most severe consequence
HGVS name

19:g.5830431delC

Variation displays