Variants in gene combination GH-LCR, SCN4A 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.4690G>A (p.Val1564Ile)	rs202106192	0.00108
NM_000334.4(SCN4A):c.3774+8G>A	rs374806849	0.00064
NM_000334.4(SCN4A):c.3001C>T (p.Arg1001Cys)	rs199713025	0.00048
NM_000334.4(SCN4A):c.4048G>A (p.Val1350Met)	rs200274258	0.00026
NM_000334.4(SCN4A):c.2704G>A (p.Gly902Ser)	rs200517944	0.00021
NM_000334.4(SCN4A):c.2563A>G (p.Met855Val)	rs372019457	0.00011
NM_000334.4(SCN4A):c.4711C>T (p.Pro1571Ser)	rs772552529	0.00005
NM_000334.4(SCN4A):c.5367G>A (p.Ser1789=)	rs189230866	0.00004
NM_000334.4(SCN4A):c.5000C>T (p.Pro1667Leu)	rs765721076	0.00001
NM_000334.4(SCN4A):c.5284G>A (p.Gly1762Arg)	rs763493738

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