ClinVar Miner

List of variants in gene DLL3 reported as likely pathogenic for autosomal recessive disease

Included ClinVar conditions (1196):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_203486.3(DLL3):c.945_946del (p.Ala317fs) rs786200900 0.00004
NM_203486.3(DLL3):c.1312T>A (p.Cys438Ser)
NM_203486.3(DLL3):c.366_378del (p.Ile123fs) rs2079604821

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