DisGeNET - a database of gene-disease associations

List of shared variants

Obesity, C0028754

Disease: Diabetes Mellitus

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
rs35439639	AVPR1B	1.000	0.080	1	206109537	3 prime UTR variant	C/G;T	snv			2
rs35608965	AVPR1B	1.000	0.080	1	206116919	5 prime UTR variant	A/G	snv	4.9E-02	6.2E-02	2
rs1269801977	PPIG	0.925	0.120	2	169604087	missense variant	A/G	snv	4.0E-06	7.0E-06	4
rs3115757	APLN	0.925	0.120	X	129648435	intron variant	C/G	snv		0.26	3
rs35457250	AHSG	0.925	0.080	3	186620775	missense variant	C/T	snv	9.0E-03	8.1E-03	5
rs757431022	SORBS1	0.925	0.120	10	95432529	missense variant	G/A	snv	1.4E-04	4.2E-05	3
rs987237	TFAP2B	0.925	0.120	6	50835337	intron variant	A/G	snv		0.17	10
rs12104705	KCNH7	0.882	0.120	2	162435107	intron variant	C/T	snv		0.15	4
rs150016118	UCP3	0.882	0.120	11	74006339	missense variant	A/G	snv	1.7E-05	6.3E-05	6
rs17700633		0.882	0.120	18	60262199	intergenic variant	G/A	snv		0.28	4
rs225015	DIO2	0.882	0.160	14	80201236	3 prime UTR variant	G/A	snv		0.37	5
rs361072	PIK3CB	0.882	0.120	3	138759702	intron variant	G/A;C	snv			4
rs3736544	TMEM165 ; CLOCK	0.882	0.160	4	55443825	synonymous variant	A/G	snv	0.70	0.69	4
rs45539933	UCP1	0.882	0.280	4	140567914	missense variant	C/T	snv	8.7E-02	7.7E-02	5
rs561017686	NEUROD1 ; CERKL	0.882	0.120	2	181678138	missense variant	G/A;C	snv	8.0E-06; 8.4E-04		4
rs6548238		0.882	0.200	2	634905	TF binding site variant	T/C	snv		0.85	10
rs753152	RAMP2-AS1 ; RAMP2	0.882	0.160	17	42761487	intron variant	T/G	snv		0.12	6
rs777659543	UCP3	0.882	0.120	11	74006231	missense variant	G/A	snv	4.0E-06		6
rs886040857	EIF2S3	0.882	0.240	X	24076757	frameshift variant	TCAA/-	delins			7
rs894160	PLIN1	0.882	0.120	15	89668592	intron variant	C/T	snv		0.29	4
rs55758736	BLK	0.851	0.120	8	11548067	missense variant	G/A	snv	1.2E-02	1.5E-02	5
rs7968585	LINC02354	0.851	0.160	12	47838310	downstream gene variant	C/G;T	snv			7
rs10010131	WFS1	0.827	0.120	4	6291188	intron variant	A/G	snv	0.66	0.63	7
rs10946398	CDKAL1	0.827	0.160	6	20660803	intron variant	A/C	snv		0.40	7
rs11196205	TCF7L2	0.827	0.200	10	113047288	intron variant	G/A;C;T	snv			7