DisGeNET - a database of gene-disease associations

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	Chr	Position	Consequence	Alleles	Class	AF GENOME	Num. diseases
rs10041590	C5orf17	5	24064827	intron variant	T/C;G	snv		2
rs10054178	C5orf17	5	24059742	intron variant	A/G	snv	7.5E-02	2
rs10056373	C5orf17	5	24069684	intron variant	C/T	snv	7.4E-02	2
rs10827209	NRP1	10	33198261	intron variant	A/C	snv	0.23	2
rs10892961	CLMP	11	123093392	intron variant	A/C;G;T	snv		2
rs11011237	TACC1P1	10	37531016	intron variant	G/A	snv	9.2E-02	2
rs11218976	CLMP	11	123090950	intron variant	A/G	snv	0.41	2
rs113051092	C5orf17	5	24060490	intron variant	A/T	snv	7.4E-02	2
rs11914494	IGSF11	3	119121264	intron variant	G/A	snv	1.8E-02	2
rs11926663	IGSF11	3	119125638	intron variant	A/G	snv	1.8E-02	2
rs141827060	IGSF11	3	119132020	intron variant	C/T	snv	1.8E-02	2
rs16893073	C5orf17	5	24072508	intron variant	C/G;T	snv		2
rs17062789	DLGAP2	8	1203198	intron variant	G/A;C	snv		2
rs17062791	DLGAP2	8	1203431	intron variant	C/T	snv	0.14	2
rs34003842	DLGAP2	8	1206131	intron variant	G/A;C;T	snv		2
rs4936770	HSPA8 ; SNORD14E	11	123058167	intron variant	C/A;T	snv		2
rs7109445	CLMP	11	123094779	intron variant	A/C;G	snv		2
rs7121616	CLMP	11	123095918	intron variant	A/G	snv	0.41	2
rs73055009	C5orf17	5	24058406	intron variant	A/G	snv	7.5E-02	2
rs73055087	C5orf17	5	24062454	intron variant	C/A;T	snv		2
rs731580	FGD5	3	14815331	intron variant	G/A	snv	0.31	2
rs73670671	DLGAP2	8	1203645	intron variant	T/C;G	snv		2
rs7696218	PACRGL	4	20721189	intron variant	G/A	snv	0.11	2
rs79056512	C5orf17	5	24063287	intron variant	G/A	snv	7.4E-02	2
rs116965780		18	43300829	intergenic variant	C/T	snv	7.0E-02	2