DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, C0011849

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
rs10494366	LOC105371475 ; NOS1AP	0.851	0.200	1	162115895	intron variant	G/T	snv		0.54	7
rs1061170	CFH	0.561	0.720	1	196690107	missense variant	C/T	snv	0.68	0.64	72
rs10911021	LOC105371642 ; LINC01344	0.807	0.160	1	182112825	intron variant	C/T	snv		0.36	11
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1458766475	C1orf112 ; SELE	0.637	0.680	1	169732649	missense variant	C/G;T	snv	4.0E-06; 4.0E-06		41
rs150924946	LMNA	0.882	0.120	1	156135271	missense variant	A/G	snv	4.8E-04	1.6E-04	5
rs17106184	FAF1	0.925	0.080	1	50444313	intron variant	G/A	snv		8.5E-02	3
rs1800871	IL19 ; IL10	0.508	0.800	1	206773289	5 prime UTR variant	A/G	snv		0.69	108
rs1800872	IL19 ; IL10	0.495	0.840	1	206773062	5 prime UTR variant	T/G	snv		0.69	119
rs1800896	IL19 ; IL10	0.507	0.800	1	206773552	intron variant	T/C	snv		0.41	113
rs1801131	MTHFR	0.535	0.840	1	11794419	missense variant	T/G	snv	0.29	0.26	93
rs1801133	MTHFR	0.472	0.880	1	11796321	missense variant	G/A	snv	0.31	0.27	174
rs1805094	LEPR	0.716	0.440	1	65610269	missense variant	G/C;T	snv	0.16; 4.0E-06		16
rs2070150	ATF6	0.827	0.280	1	161791486	missense variant	G/C	snv	0.14	9.2E-02	6
rs2146727	POU2F1	0.925	0.080	1	167312910	intron variant	G/A	snv		0.56	3
rs2228145	IL6R	0.602	0.720	1	154454494	missense variant	A/C;T	snv	0.38; 1.2E-05		57
rs2275558	PBX1	0.882	0.200	1	164559883	missense variant	G/A	snv	0.30	0.19	5
rs2275703	CASQ1	0.925	0.080	1	160195305	intron variant	A/C	snv		0.38	3
rs2476601	AP4B1-AS1 ; PTPN22	0.498	0.800	1	113834946	missense variant	A/G	snv	0.93	0.93	121
rs2890565	UTS2	0.732	0.440	1	7849677	missense variant	C/T	snv	8.7E-02	5.6E-02	15
rs3767140	HSPG2	1.000	0.080	1	21888152	intron variant	C/A	snv		0.25	3
rs3767434	POU2F1	0.925	0.080	1	167401914	intron variant	T/C	snv		0.14	3
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs4641	LMNA	0.851	0.120	1	156137743	splice region variant	C/T	snv	0.26	0.21	6
rs4762	AGT	0.637	0.440	1	230710231	missense variant	G/A	snv	0.12	0.11	35