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	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs10004195	TLR10	0.790	0.320	4	38783103	upstream gene variant	T/A	snv		0.29	8
rs10008032	LOC105374413	1.000	0.080	4	38743861	intergenic variant	T/C	snv		0.66	2
rs10008492		1.000	0.120	4	38764099	intergenic variant	C/G;T	snv			2
rs10024216				4	38762491	upstream gene variant	G/A	snv		0.37	1
rs10033073	STX18-AS1 ; LOC101928279			4	4773674	intron variant	A/G	snv		0.32	1
rs10034903	TLR10			4	38783057	upstream gene variant	C/G	snv		0.35	1
rs10038058	WDR36			5	111107582	intron variant	A/G	snv		0.54	1
rs10038177	WDR36	0.925	0.040	5	111100751	intron variant	C/T	snv	0.53	0.54	3
rs10041894				5	40493132	intron variant	G/A;C	snv			1
rs10043301	TTC33			5	40530784	intron variant	C/T	snv		0.64	1
rs10045255	WDR36			5	111102658	intron variant	A/G	snv		0.55	1
rs10051830	WDR36			5	111117147	intron variant	G/A;T	snv			1
rs10055177	WDR36			5	111114886	intron variant	T/G	snv		0.53	1
rs10055860	TTC33			5	40569851	intron variant	C/G;T	snv			1
rs10056340		0.925	0.080	5	110854353	intergenic variant	T/G	snv		0.31	3
rs10060003	WDR36			5	111113658	intron variant	A/G	snv		0.53	1
rs10068204	TTC33			5	40519249	intron variant	T/C	snv		0.63	1
rs10068717	NDFIP1			5	142115369	intron variant	C/T	snv		0.67	1
rs10074523	KIF3A	1.000	0.080	5	132724891	intron variant	C/A	snv		0.62	2
rs10075020	TTC33			5	40575737	intron variant	T/A;C	snv			1
rs10076944				5	40496849	intron variant	G/A	snv		0.60	1
rs1008723	GSDMB	0.925	0.160	17	39910014	intron variant	G/C;T	snv			3
rs10114457				9	6130940	intergenic variant	A/G	snv		0.81	1
rs10166330	IL18RAP			2	102433930	intron variant	C/T	snv		0.22	1
rs10167431	IL1RL2			2	102236342	intron variant	T/C	snv		0.55	1