"Clinical Genetics, Academic Medical Center"[submitter] AND "SCN3B"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 642346	NM_001040151.2(SCN3B):c.583G>A (p.Ala195Thr)	SCN3B (A195T)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +3 more	GConflicting classifications of pathogenicity
Select item 190883	NM_001040151.2(SCN3B):c.582C>T (p.Asn194=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +2 more	GBenign/Likely benign
Select item 1129101	NM_001040151.2(SCN3B):c.570A>G (p.Ala190=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +1 more	GLikely benign
Select item 139033	NM_001040151.2(SCN3B):c.390G>A (p.Ala130=)	SCN3B	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 190886	NM_001040151.2(SCN3B):c.328G>A (p.Val110Ile)	SCN3B (V110I)	Single nucleotide variant (missense variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 190885	NM_001040151.2(SCN3B):c.198C>T (p.Pro66=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +3 more	GBenign
Select item 1005948	NM_001040151.2(SCN3B):c.73G>T (p.Val25Leu)	SCN3B (V25L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar