"Clinical Genetics, Academic Medical Center"[submitter] AND "LOC105370 - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1299905	NM_005477.3(HCN4):c.1162C>T (p.Leu388=)	HCN4, LOC105370890 +1 more	Single nucleotide variant (synonymous variant)	Brugada syndrome 8	GLikely benign
Select item 190779	NM_005477.3(HCN4):c.1132C>T (p.Arg378Cys)	HCN4, LOC105370890 +1 more (R378C)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 412784	NM_005477.3(HCN4):c.1090G>A (p.Asp364Asn)	LOC126862173, HCN4 +1 more (D364N)	Single nucleotide variant (missense variant)	Sick sinus syndrome 2, autosomal dominant +3 more	GBenign/Likely benign
Select item 412787	NM_005477.3(HCN4):c.1089C>T (p.Ile363=)	HCN4, LOC105370890 +1 more	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1174971	NM_005477.3(HCN4):c.1053C>T (p.Pro351=)	HCN4, LOC105370890 +1 more	Single nucleotide variant (synonymous variant)	Brugada syndrome 8	GLikely benign

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