DisGeNET - a database of gene-disease associations

List of associated variants

Pulmonary function (finding), C3160731

Source: GWASDB ×

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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	Num. diseases
rs12914385	CHRNA3	0.790	0.160	15	78606381	intron variant	C/A;T	snv		8
rs2284746	MFAP2			1	16980180	intron variant	C/A;G	snv		4
rs12477314				2	238955452	regulatory region variant	C/G;T	snv		3
rs1529672	RARB	1.000	0.040	3	25479091	intron variant	C/A;T	snv		3
rs2571445	TNS1	0.925	0.080	2	217818431	missense variant	A/G;T	snv	0.62	3
rs2904259	FAM13A			4	88964563	intron variant	T/A;C	snv		3
rs7733088	HTR4 ; LOC107986462	1.000	0.040	5	148476770	intron variant	G/A;C	snv	0.44; 4.1E-06	3
rs7741741	ADGRG6	0.925	0.040	6	142334664	intron variant	T/A;G	snv		3
rs8192575	NOTCH4	1.000	0.120	6	32198607	intron variant	C/G;T	snv	7.0E-02; 4.1E-06	3
rs1040525	ADGRG6			6	142382532	intron variant	C/A;G;T	snv		2
rs10463406	LOC107986462 ; HTR4			5	148459281	intron variant	C/A;T	snv		2
rs10866659	ADAM19	1.000	0.040	5	157510035	intron variant	A/G;T	snv		2
rs11257613	CDC123			10	12242393	intron variant	G/A;C	snv		2
rs113096699	ADGRG6			6	142424746	intron variant	-/G	ins		2
rs11598305	CDC123			10	12227401	intron variant	C/A;G	snv		2
rs11732650	GSTCD ; INTS12			4	105833074	intron variant	G/A;C	snv		2
rs11736859	GSTCD ; INTS12 ; GSTCD-AS1			4	105787628	intron variant	C/G;T	snv		2
rs1344555	MECOM			3	169582431	intron variant	C/A;G;T	snv		2
rs1422795	ADAM19			5	157509356	missense variant	T/C;G	snv	0.38; 8.0E-06	2
rs1489762	LOC105377462			4	144533812	intron variant	T/C;G	snv		2
rs153916	SPATA9	1.000	0.040	5	95700996	upstream gene variant	C/A;G;T	snv		2
rs1541374				4	105127203	intergenic variant	T/A;G	snv		2
rs16825267	LINC01807 ; LOC105373920	1.000	0.040	2	228705203	intron variant	C/A;G	snv		2
rs16909856				9	95442211	downstream gene variant	G/A;C;T	snv		2
rs17035960	ARHGEF38			4	105610689	intron variant	C/A;T	snv		2