DisGeNET - a database of gene-disease associations

List of associated variants

Coronary Artery Disease, C1956346

Source: GWASCAT ×

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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
rs36096196	MORN1	1.000	0.040	1	2320766	non coding transcript exon variant	C/T	snv		0.11	1
rs3931020		0.882	0.040	1	74769633	downstream gene variant	T/C	snv		0.71	1
rs4072980	SF3A3	1.000	0.040	1	37990434	upstream gene variant	G/A;C	snv			1
rs4537545	IL6R	0.790	0.160	1	154446403	intron variant	C/T	snv		0.48	1
rs4634932	PLPP3	1.000	0.040	1	56530519	intron variant	T/C	snv		7.2E-02	1
rs4845570	TDRKH	1.000	0.040	1	151786628	intron variant	C/T	snv		0.79	1
rs4845625	IL6R	0.851	0.080	1	154449591	intron variant	T/C	snv		0.60	1
rs5063	CLCN6 ; NPPA-AS1 ; NPPA	0.763	0.280	1	11847591	missense variant	C/T	snv	5.6E-02	5.3E-02	1
rs56170783	PLPP3	1.000	0.040	1	56550459	intron variant	A/C	snv		6.5E-02	1
rs60154123	LINC02602	1.000	0.040	1	210295654	intergenic variant	C/T	snv		0.12	1
rs611917	CELSR2	1.000	0.040	1	109272630	non coding transcript exon variant	A/G	snv	0.28	0.32	1
rs6700559	DDX59-AS1	1.000	0.040	1	200676945	intron variant	C/T	snv		0.43	1
rs67180937	MIA3	1.000	0.040	1	222650401	intron variant	T/C;G	snv	0.64		1
rs72664324	PLPP3	1.000	0.040	1	56506681	intron variant	G/A	snv		0.10	1
rs7553007		0.827	0.120	1	159728759	intergenic variant	G/A	snv		0.31	1
rs852787	DAB1	1.000	0.040	1	57836430	intron variant	C/T	snv		0.16	1
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	35
rs780093	GCKR	0.763	0.240	2	27519736	intron variant	T/C	snv		0.68	16
rs715	CPS1	1.000	0.040	2	210678331	3 prime UTR variant	T/C	snv		0.28	10
rs2571445	TNS1	0.925	0.080	2	217818431	missense variant	A/G;T	snv	0.62		8
rs887829	UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9	0.763	0.280	2	233759924	intron variant	C/T	snv		0.36	8
rs2972146		0.882	0.040	2	226235982	intergenic variant	G/T	snv		0.72	6
rs4299376	LOC102725159 ; ABCG8	0.851	0.120	2	43845437	intron variant	G/C;T	snv			6
rs1250259	FN1 ; LOC105373868	1.000	0.040	2	215435759	missense variant	T/A	snv	0.76	0.79	5
rs2943634		0.763	0.200	2	226203364	intergenic variant	A/C;G	snv			5