Variants in gene SCN1B with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser)	rs72552027	0.00249
NM_001037.5(SCN1B):c.448+193G>A	rs66876876	0.00227
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr)	rs150721582	0.00021
NM_001037.5(SCN1B):c.449-3C>A	rs370937269	0.00007
NM_001037.5(SCN1B):c.415G>A (p.Val139Ile)	rs560827790	0.00006
NM_001037.5(SCN1B):c.561C>T (p.Ala187=)	rs587781152	0.00005
NM_001037.5(SCN1B):c.23T>C (p.Val8Ala)	rs786205833	0.00003
NM_001037.5(SCN1B):c.367G>A (p.Val123Ile)	rs754215948	0.00002
NM_001037.5(SCN1B):c.150C>T (p.Asn50=)	rs147073518	0.00001
NM_001037.5(SCN1B):c.266G>A (p.Arg89His)	rs138381632	0.00001
NM_001037.5(SCN1B):c.273G>A (p.Val91=)	rs16969926	0.00001
NM_001037.5(SCN1B):c.640G>A (p.Val214Ile)	rs77106213	0.00001
NM_001037.5(SCN1B):c.522C>A (p.Leu174=)	rs35478147

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