List of variants in gene SCN8A reported by GenomeConnect, ClinGen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.2287A>G (p.Ile763Val)	rs794727128
NM_001330260.2(SCN8A):c.3942+2_3942+5dup	rs764867016
NM_001330260.2(SCN8A):c.4146_4147dup (p.Asn1383fs)	rs1555228380
NM_001330260.2(SCN8A):c.550A>G (p.Ile184Val)	rs1029149299

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