Variants in gene combination LOC102724058, SCN1A with conflicting interpretations reported as "uncertain significance and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3521C>G (p.Thr1174Ser)	rs121918799	0.00159
NM_001165963.4(SCN1A):c.5951C>A (p.Pro1984His)	rs146733308	0.00074
NM_001165963.4(SCN1A):c.3924A>T (p.Glu1308Asp)	rs121917910	0.00070
NM_001165963.4(SCN1A):c.4872G>A (p.Leu1624=)	rs142910512	0.00048
NM_001165963.4(SCN1A):c.5568G>A (p.Met1856Ile)	rs144691638	0.00038
NM_001165963.4(SCN1A):c.4887C>T (p.Phe1629=)	rs587780445	0.00008
NM_001165963.4(SCN1A):c.3481G>A (p.Ala1161Thr)	rs201079458	0.00006
NM_001165963.4(SCN1A):c.4724G>A (p.Arg1575His)	rs368834365	0.00006
NM_001165963.4(SCN1A):c.4556C>T (p.Pro1519Leu)	rs372425457	0.00004
NM_001165963.4(SCN1A):c.4723C>T (p.Arg1575Cys)	rs121918807	0.00003
NM_001165963.4(SCN1A):c.5346C>T (p.Ile1782=)	rs121918763	0.00001
NM_001165963.4(SCN1A):c.3705+10del	rs570862962

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