Original source

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

Alleles
CCGA/- | MAF: 0.01 (-)
Location

Chromosome 17:42111729-42111732 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.42111729_42111732delCCGA

Variation displays