List of variants in gene combination SCN1A, SCN9A reported as likely benign for complex neurodevelopmental disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.2875-5del	rs774840081	0.00011
NM_001365536.1(SCN9A):c.1605_1606del	rs200091138
NM_001365536.1(SCN9A):c.1960_1962dup	rs202073550
NM_001365536.1(SCN9A):c.1975-3del	rs35888674

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