DisGeNET - a database of gene-disease associations

List of associated variants

Sudden Cardiac Death, C0085298

Source: ALL

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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
rs16942421	KCTD1			18	26576461	intron variant	G/A;T	snv			2
rs12429889	KLF12			13	74168185	intergenic variant	T/C	snv		0.29	2
rs7307780	LOC105369844			12	75826838	intron variant	C/T	snv		0.18	2
rs9581094	LOC105370117 ; TPTE2P6 ; PARP4			13	24508492	intron variant	T/C	snv		0.13	2
rs4621553	LOC107986441			5	113694467	intergenic variant	G/A	snv		0.78	2
rs10765792	MAML2			11	96133536	intron variant	G/C	snv		0.10	2
rs11187837	PLCE1			10	94276223	intron variant	T/C	snv		8.4E-02	2
rs13022357	TANC1			2	159213245	intron variant	A/G	snv		0.83	2
rs10183640	UPP2			2	157923692	intron variant	G/A	snv		0.31	2
rs16872085	ZFPM2			8	104945312	intron variant	A/G	snv		7.6E-02	2
rs16866933	ZNF385B ; LOC107985967			2	179701951	intron variant	G/A	snv		9.3E-02	2
rs1554218	NGEF			2	232894174	intron variant	G/T	snv		8.9E-02	1
rs6730157	RAB3GAP1 ; ZRANB3			2	135149518	intron variant	A/G	snv		0.60	1
rs71352737	TRPM4			19	49182889	stop gained	G/A	snv	1.5E-03	1.6E-03	1
rs2077316	ZNF365			10	62465689	intron variant	A/C;T	snv			1