DisGeNET - a database of gene-disease associations

List of shared variants

Parkinson Disease, C0030567

Disease: Hypertensive disease

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
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs1169089134	FOLH1	0.790	0.320	11	49206785	missense variant	C/G;T	snv			9
rs1206846668	FOLH1	0.724	0.400	11	49185773	missense variant	G/A	snv	4.1E-06		16
rs1279844744	CYP1A1	0.925	0.080	15	74720521	missense variant	A/G	snv			3
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		34
rs1544410	VDR	0.542	0.760	12	47846052	intron variant	C/A;G;T	snv			78
rs2228570	VDR	0.521	0.760	12	47879112	start lost	A/C;G;T	snv	0.63		99
rs368087026	SLC19A1	0.637	0.520	21	45530890	missense variant	G/A	snv			33
rs3836790	SLC6A3	0.882	0.080	5	1411740	intron variant	-/ACATACACACTCAGACACACATACCATGCA	ins			5
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs4588	GC	0.597	0.720	4	71752606	missense variant	G/A;T	snv	1.6E-05; 0.25		53
rs5569	SLC6A2	0.742	0.280	16	55697923	synonymous variant	G/A;C	snv	0.31; 4.0E-06		19
rs699947	VEGFA	0.570	0.680	6	43768652	upstream gene variant	A/C;T	snv			67
rs7041	GC	0.576	0.800	4	71752617	missense variant	A/C;T	snv	0.52; 4.0E-06		64
rs755001634	FOLH1	0.763	0.280	11	49154384	stop gained	G/A	snv	1.2E-05		13
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237
rs763059810	CXCR4	0.623	0.600	2	136115750	missense variant	T/C	snv	4.0E-06		41
rs765545512	HFE	0.827	0.240	6	26093226	missense variant	G/A;T	snv	4.0E-06; 1.6E-05		6
rs953038635	SOD2	0.590	0.800	6	159692720	missense variant	G/A;T	snv	8.0E-06		51
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1416580204	MOK	0.608	0.720	14	102250837	missense variant	C/T	snv	4.0E-06	7.0E-06	49
rs1368310331	CYP1A1	0.827	0.200	15	74723032	synonymous variant	T/C	snv		7.0E-06	6
rs28363170	SLC6A3	0.827	0.120	5	1393745	3 prime UTR variant	-/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC	delins		8.1E-06	7
rs893924483	BDNF ; BDNF-AS	0.716	0.280	11	27658285	missense variant	C/A;T	snv	4.0E-06	1.4E-05	23
rs368939818	FOLH1	0.763	0.280	11	49156734	missense variant	G/A	snv	4.0E-05	2.1E-05	13