DisGeNET - a database of gene-disease associations

List of associated variants

Diabetes Mellitus, Non-Insulin-Dependent, C0011860

Source: ALL

Results per page

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
rs2281939	SORBS1	0.790	0.320	10	95414595	missense variant	T/C	snv	8.2E-02	0.13	9
rs12026	PON2	0.827	0.240	7	95411704	missense variant	G/C	snv	0.27	0.27	6
rs7493	PON2	0.677	0.440	7	95405463	missense variant	G/C	snv	0.27	0.27	24
rs854560	PON1	0.513	0.800	7	95316772	missense variant	A/C;G;N;T	snv	0.29		113
rs13306698	PON1	0.882	0.240	7	95311470	missense variant	T/C	snv	6.0E-03	1.9E-03	3
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157
rs13078	DICER1	0.827	0.280	14	95090410	3 prime UTR variant	A/T	snv		0.85	5
rs3742330	DICER1	0.662	0.640	14	95087025	3 prime UTR variant	A/G	snv		8.7E-02	24
rs11572080	CYP2C8	0.882	0.160	10	95067273	missense variant	C/A;T	snv	8.3E-02		4
rs540288649	CYP2C8	1.000	0.080	10	95067259	missense variant	G/A;C	snv	1.6E-05; 7.2E-04		1
rs11572103	CYP2C8	0.851	0.120	10	95058349	missense variant	T/A	snv	1.6E-02	4.9E-02	4
rs1057910	CYP2C9	0.776	0.280	10	94981296	missense variant	A/C;G	snv	6.3E-02; 4.0E-06		12
rs1320164	TP53INP1 ; NDUFAF6	1.000	0.080	8	94948539	intron variant	G/A	snv		0.45	1
rs896854	TP53INP1 ; NDUFAF6	1.000	0.080	8	94948283	intron variant	T/C	snv		0.45	2
rs1799853	CYP2C9	0.763	0.320	10	94942290	missense variant	C/T	snv	9.2E-02	8.9E-02	11
rs7845219	NDUFAF6	1.000	0.080	8	94925274	intron variant	T/C	snv		0.45	1
rs17359493	INTS8	1.000	0.080	8	94844683	intron variant	A/G	snv		0.19	1
rs11097432	PDLIM5	1.000	0.080	4	94658554	intron variant	T/C	snv		0.24	2
rs7542900	LOC105378861	1.000	0.080	1	94604485	intergenic variant	T/C	snv		0.74	1
rs12500426	PDLIM5	0.851	0.240	4	94593458	intron variant	A/C	snv		0.54	5
rs2236242	SERPINA12	0.776	0.280	14	94493715	intron variant	T/A	snv		0.31	9
rs7214842	STX8	1.000	0.080	17	9445693	intron variant	C/T	snv		0.71	1
rs10114341	LOC107987099	1.000	0.080	9	94156900	non coding transcript exon variant	T/C	snv		0.42	1
rs61748537	ABCA4	0.882	0.160	1	94098906	missense variant	C/G;T	snv	4.0E-05; 8.0E-06		3
rs3758539	FFAR4 ; RBP4	0.925	0.120	10	93601831	intron variant	C/T	snv		0.13	4