Variants in gene SCN2A with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 22

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.2548C>T (p.Arg850Ter)	rs1553578503
NM_001040142.2(SCN2A):c.2558G>A (p.Arg853Gln)	rs794727152
NM_001040142.2(SCN2A):c.2567G>A (p.Arg856Gln)	rs797045942
NM_001040142.2(SCN2A):c.2642T>C (p.Leu881Pro)	rs796053116
NM_001040142.2(SCN2A):c.2654C>T (p.Thr885Ile)	rs1699477928
NM_001040142.2(SCN2A):c.2674G>A (p.Val892Ile)	rs121917751
NM_001040142.2(SCN2A):c.2995G>A (p.Glu999Lys)	rs796053126
NM_001040142.2(SCN2A):c.3631G>A (p.Glu1211Lys)	rs387906684
NM_001040142.2(SCN2A):c.3947C>T (p.Ala1316Val)	rs796053130
NM_001040142.2(SCN2A):c.3955C>T (p.Arg1319Trp)	rs190111194
NM_001040142.2(SCN2A):c.3956G>A (p.Arg1319Gln)
NM_001040142.2(SCN2A):c.4886G>A (p.Arg1629His)
NM_001040142.2(SCN2A):c.4904G>A (p.Arg1635Gln)	rs1057520844
NM_001040142.2(SCN2A):c.4976C>T (p.Ala1659Val)	rs1060503101
NM_001040142.2(SCN2A):c.5317G>A (p.Ala1773Thr)	rs796053162
NM_001040142.2(SCN2A):c.5636T>C (p.Met1879Thr)	rs2105403536
NM_001040142.2(SCN2A):c.5645G>A (p.Arg1882Gln)	rs794727444
NM_001040142.2(SCN2A):c.605C>T (p.Ala202Val)
NM_001040142.2(SCN2A):c.751G>A (p.Val251Ile)	rs1057519528
NM_001040142.2(SCN2A):c.781G>A (p.Val261Met)	rs1057520413
NM_001040142.2(SCN2A):c.843G>A (p.Trp281Ter)
NM_001371246.1(SCN2A):c.634A>G (p.Asn212Asp)	rs1553567473

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