DisGeNET - a database of gene-disease associations

List of shared variants

Calcification of coronary artery, C1611184

Disease: Diabetes Mellitus, Non-Insulin-Dependent

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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs1333049	CDKN2B-AS1	0.614	0.520	9	22125504	intron variant	G/C	snv		0.41	60
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	47
rs10757278	CDKN2B-AS1	0.620	0.520	9	22124478	intron variant	A/G	snv		0.40	44
rs4977574	CDKN2B-AS1	0.695	0.520	9	22098575	intron variant	A/G;T	snv			26
rs1063192	CDKN2B ; CDKN2B-AS1	0.695	0.520	9	22003368	3 prime UTR variant	G/A;T	snv			24
rs10757274	CDKN2B-AS1	0.701	0.320	9	22096056	intron variant	A/G	snv		0.41	22
rs2383207	CDKN2B-AS1	0.695	0.280	9	22115960	intron variant	A/G	snv		0.64	22
rs560887	SPC25 ; G6PC2	0.827	0.120	2	168906638	intron variant	T/C	snv	0.79	0.80	18
rs564398	CDKN2B-AS1	0.716	0.360	9	22029548	3 prime UTR variant	T/C	snv	0.31	0.28	18
rs2383206	CDKN2B-AS1	0.742	0.320	9	22115027	intron variant	A/G	snv		0.49	17
rs1333045	CDKN2B-AS1	0.776	0.280	9	22119196	non coding transcript exon variant	T/C	snv		0.50	14
rs1412829	CDKN2B-AS1	0.742	0.400	9	22043927	intron variant	A/G	snv		0.28	14
rs10738610	CDKN2B-AS1	0.882	0.120	9	22123767	intron variant	A/C;T	snv			5
rs2891168	CDKN2B-AS1	0.851	0.160	9	22098620	intron variant	A/G	snv		0.40	5
rs1440581	PPM1K-DT	1.000	0.080	4	88305270	intron variant	T/A;C	snv			4
rs944801	CDKN2B-AS1	0.882	0.120	9	22051671	intron variant	G/A;C	snv			4
rs10978777		1.000	0.080	9	107268309	intergenic variant	G/A;C	snv			2
rs113533135	LRP1B	1.000	0.080	2	140268867	intron variant	T/C	snv		2.0E-02	2
rs113805659	MAGI2	1.000	0.080	7	78663475	intron variant	G/C	snv		6.1E-02	2
rs114031744		1.000	0.080	10	123610085	intergenic variant	A/G	snv		1.7E-02	2
rs11509197		1.000	0.080	7	118641356	intergenic variant	C/T	snv		0.38	2
rs115689251	LOC107985068	1.000	0.080	17	36032377	intergenic variant	A/C	snv		1.0E-02	2
rs117854110		1.000	0.080	7	105603002	upstream gene variant	C/A;T	snv			2
rs12040333	ST3GAL3	1.000	0.080	1	43848369	intron variant	G/A;C	snv			2