DisGeNET - a database of gene-disease associations

List of associated variants

Diabetic Nephropathy, C0011881

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
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs805304	CLIC1 ; DDAH2	0.851	0.240	6	31730311	5 prime UTR variant	T/G	snv		0.48	5
rs11107616	NAV3	1.000	0.120	12	77971000	intron variant	T/G	snv		0.13	1
rs7639705	MCF2L2	1.000	0.120	3	183309754	missense variant	T/G	snv	0.26	0.27	1
rs2241766	ADIPOQ ; ADIPOQ-AS1	0.608	0.720	3	186853103	synonymous variant	T/C;G	snv	8.0E-06; 0.13		48
rs652438	MMP12	0.716	0.400	11	102865911	missense variant	T/C;G	snv	7.1E-02; 2.5E-04		14
rs25487	XRCC1	0.441	0.800	19	43551574	missense variant	T/C	snv	0.68	0.71	205
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157
rs1800896	IL19 ; IL10	0.507	0.800	1	206773552	intron variant	T/C	snv		0.41	113
rs1267969615	ACE	0.532	0.760	17	63490960	missense variant	T/C	snv	4.0E-06		100
rs429358	APOE	0.590	0.600	19	44908684	missense variant	T/C	snv	0.14	0.16	66
rs1799964	LTA ; LOC100287329 ; TNF	0.608	0.760	6	31574531	upstream gene variant	T/C	snv		0.19	47
rs10811661		0.724	0.400	9	22134095	intergenic variant	T/C	snv		0.14	22
rs12976445	SPACA6 ; SPACA6P-AS ; MIRLET7E ; MIR125A	0.689	0.600	19	51693200	non coding transcript exon variant	T/C	snv		0.45	20
rs7679	PCIF1	0.925	0.160	20	45947863	3 prime UTR variant	T/C	snv		0.13	9
rs1549758	NOS3	0.807	0.360	7	150998638	synonymous variant	T/C	snv	0.76	0.76	7
rs3752462	MYH9	0.827	0.160	22	36314138	splice region variant	T/C	snv	0.57	0.53	7
rs11651270	NLRP1	0.882	0.240	17	5521757	missense variant	T/C	snv	0.45	0.47	4
rs2779248	NOS2	0.882	0.160	17	27800806	intron variant	T/C	snv		0.39	4
rs1567438	LPAL2	0.925	0.200	6	160458599	intron variant	T/C	snv		0.25	3
rs4311	ACE	0.882	0.200	17	63483402	intron variant	T/C	snv		0.60	3
rs11538209	ALB	1.000	0.120	4	73404356	missense variant	T/C	snv			2
rs3796268	MME	0.925	0.200	3	155117435	intron variant	T/C	snv		0.30	2
rs488846		0.925	0.160	18	54261400	intergenic variant	T/C	snv		0.26	2
rs762285755	CUBN	0.925	0.160	10	17114074	missense variant	T/C	snv	7.6E-05	2.8E-05	2