DisGeNET - a database of gene-disease associations

List of shared variants

Cardiomyopathy, Familial Hypertrophic, 1 (disorder), C3495498

Disease: Wolff-Parkinson-White Syndrome

Source: CLINVAR ×

Results per page

Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs3218716	MYH7	0.716	0.280	14	23425316	missense variant	C/A;G;T	snv	4.0E-06; 2.4E-05		17
rs267606910	MYH7	0.807	0.080	14	23431589	missense variant	C/T	snv	8.0E-06		5