DisGeNET - a database of gene-disease associations

Source: GWASDB ×

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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
rs16899524	MICA-AS1	6	31394533	non coding transcript exon variant	C/T	snv	0.10	2
rs17496549	HLA-DRA	6	32441931	intron variant	C/T	snv	0.10	2
rs2294882	TSBP1-AS1 ; BTNL2	6	32399738	intron variant	T/C	snv	0.19	2
rs4851005	IL18R1	2	102395092	intron variant	C/T	snv	0.29	2
rs10024216		4	38762491	upstream gene variant	G/A	snv	0.37	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
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
rs10060003	WDR36	5	111113658	intron variant	A/G	snv	0.53	1
rs10068204	TTC33	5	40519249	intron variant	T/C	snv	0.63	1
rs10075020	TTC33	5	40575737	intron variant	T/A;C	snv		1
rs10076944		5	40496849	intron variant	G/A	snv	0.60	1
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
rs10170583	IL18R1	2	102358304	intron variant	G/A	snv	0.45	1
rs10172039	IL1R1	2	102122325	intron variant	C/A	snv	0.18	1
rs10172116		2	102471113	upstream gene variant	C/G;T	snv		1
rs10176664	IL18R1	2	102359712	intron variant	G/A;C	snv		1
rs10176820	IL18RAP	2	102437960	intron variant	T/C	snv	0.24	1