C1142166[trait identifier] AND "Phosphorus, Inc."[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 192099	NM_001267550.2(TTN):c.266C>G (p.Ala89Gly)	TTN (A89G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 418471	NM_006514.4(SCN10A):c.4849G>T (p.Val1617Phe)	SCN10A (V1617F +2 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 260135	NM_001377540.1(SLMAP):c.828+11C>A	SLMAP	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 45399	NM_020297.4(ABCC9):c.2093-7T>C	ABCC9	Single nucleotide variant (intron variant)	ABCC9-related condition +6 more	GConflicting classifications of pathogenicity
Select item 179026	NM_001005242.3(PKP2):c.1379-2019C>T	PKP2 (R490W)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +9 more	GConflicting classifications of pathogenicity
Select item 488177	NM_017636.4(TRPM4):c.1690C>T (p.Leu564Phe)	TRPM4 (L564F +4 more)	Single nucleotide variant (missense variant)	Brugada syndrome	GUncertain significance

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