"Baylor Genetics"[submitter] AND "SCN2B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 191495	NM_004588.5(SCN2B):c.44C>T (p.Thr15Met)	SCN2B (T15M)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 14 +2 more	GUncertain significance
Select item 625808	GRCh37/hg19 11q23.3-25(chr11:116700253-134904063)	BACE1, BACE1-AS +176 more	Copy number gain	not provided	GPathogenic
Select item 625659	GRCh37/hg19 11q23.3-25(chr11:116691675-134889485)	ARHGAP32, ARHGEF12 +177 more	Copy number gain	not provided	GPathogenic

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