ClinVar Miner

List of variants studied for benign familial infantile epilepsy by NeuroMeGen, Hospital Clinico Santiago de Compostela

Included ClinVar conditions (18):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NC_000002.11:g.(?_166152283)_(166246384_?)dup
NM_001040142.2(SCN2A):c.5117G>C (p.Cys1706Ser) rs1553463513
NM_001040142.2(SCN2A):c.5551C>T (p.Arg1851Trp) rs1553463718
NM_145239.3(PRRT2):c.649dup (p.Arg217fs)

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