Conduction Disorder of the Heart

Cardiovascular 19 variants 15 genes

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Associated Genes (15)

TRPM4 CACNA1C FLNC RYR2 CASQ2 SCN5A JUP DMD ANK2 MYH6 RBM20 DSG2 KCNH2 ABCC9 PKP2

Associated Variants (19)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS150391806	TRPM4	—	—	strong
RS2052999161	CACNA1C	—	—	strong
RS1808809268	FLNC	—	—	strong
RS1688456281	RYR2	—	—	strong
RS750159744	CASQ2	—	—	strong
RS1575703249	SCN5A	—	—	strong
RS1572627115	RYR2	—	—	strong
RS150245906	JUP	—	—	strong
RS748937055	DMD	—	—	strong
RS201693280	ANK2	—	—	strong
RS72544141	ANK2	—	—	strong
RS878854502	MYH6	—	—	strong
RS372567331	RBM20	—	—	strong
RS370316475	DSG2	—	—	strong
RS200318013	RYR2	—	—	strong
RS199473603	SCN5A	—	—	strong
RS139544114	KCNH2	—	—	strong
RS150036969	ABCC9	—	—	strong
RS149542398	PKP2	—	—	strong