Original source

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

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

Chromosome 17:44034361-44034364 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.44034361_44034364delCCGA

Variation displays