DisGeNET - a database of gene-disease associations

List of shared variants

Dementia, C0497327

Disease: Parkinson Disease

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
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs1289324472	GBA	0.716	0.400	1	155236354	missense variant	T/C	snv		1.4E-05	21
rs1805087	MTR	0.496	0.800	1	236885200	missense variant	A/G	snv	0.20	0.21	135
rs2230288	GBA	0.776	0.160	1	155236376	missense variant	C/T	snv	1.0E-02	1.0E-02	18
rs367543041	TARDBP	0.742	0.200	1	11022553	missense variant	G/A;C	snv	3.0E-05		15
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs76763715	GBA	0.658	0.520	1	155235843	missense variant	T/C;G	snv	2.3E-03		35
rs16944	IL1B	0.531	0.920	2	112837290	upstream gene variant	A/G	snv		0.57	92
rs334558	LOC107986119 ; GSK3B	0.701	0.320	3	120094435	upstream gene variant	A/G	snv		0.51	20
rs104893875	SNCA	0.742	0.120	4	89828170	missense variant	C/T	snv	4.0E-06		13
rs104893877	SNCA	0.614	0.360	4	89828149	missense variant	C/T	snv			59
rs11931074	SNCA ; LOC105377329	0.851	0.080	4	89718364	intron variant	G/A;C;T	snv			7
rs201106962	SNCA	0.851	0.080	4	89828156	missense variant	A/C	snv	8.0E-05	7.0E-05	5
rs6347	SLC6A3	0.851	0.080	5	1411297	synonymous variant	T/C	snv	0.23	0.32	4
rs1801474	PRKN	0.851	0.080	6	162201165	missense variant	C/T	snv	7.1E-02	5.3E-02	4
rs2070600	AGER	0.561	0.760	6	32183666	missense variant	C/T	snv	5.3E-02	3.6E-02	82
rs75932628	LOC105375056 ; TREM2	0.662	0.480	6	41161514	missense variant	C/A;T	snv	6.8E-05; 2.6E-03		28
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157
rs854560	PON1	0.513	0.800	7	95316772	missense variant	A/C;G;N;T	snv	0.29		113
rs11136000	CLU	0.752	0.160	8	27607002	intron variant	T/C	snv		0.56	19
rs121909330	VCP	0.752	0.200	9	35065364	missense variant	G/A;C;T	snv			11
rs121909334	VCP	0.752	0.200	9	35065255	missense variant	C/T	snv	1.6E-05		10
rs3764435	ALDH1A1	0.827	0.120	9	72901960	intron variant	A/C;T	snv			5
rs2281983	PITX3	0.851	0.080	10	102231624	missense variant	G/A;C;T	snv	0.62; 8.3E-06		4
rs2306604	TFAM	0.827	0.080	10	58388932	intron variant	A/C;G;T	snv			5