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
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	272
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237
rs9829896	KAT2B ; MIR3135A			3	20135980	intron variant	C/A;T	snv			2
rs2377339	NCK2			2	105840835	intron variant	A/G	snv		4.8E-02	2
rs12043259	NFASC			1	204858913	intron variant	C/G	snv		0.11	2
rs12284594	PKNOX2	1.000	0.080	11	125309957	intron variant	A/G;T	snv			2
rs118129027				7	39545812	non coding transcript exon variant	T/C	snv		3.5E-02	1
rs1417205				13	47324744	intergenic variant	A/G	snv		0.13	1
rs12995333	NCK2			2	105819909	intron variant	G/T	snv		0.30	1
rs12995849	NCK2			2	105826655	intron variant	C/T	snv		0.63	1
rs1465639	NCK2			2	105822725	intron variant	T/C	snv		0.32	1
rs1465641	NCK2			2	105822480	intron variant	C/G;T	snv			1
rs2163349	NCK2			2	105841192	intron variant	A/G	snv		0.30	1
rs2163350	NCK2			2	105828825	intron variant	A/C;G	snv			1
rs4851095	NCK2			2	105839093	intron variant	T/C	snv		0.94	1
rs4851870	NCK2			2	105820800	intron variant	C/T	snv		0.20	1
rs6741172	NCK2			2	105823603	intron variant	A/G	snv		0.32	1
rs6747023	NCK2			2	105815399	intron variant	A/G;T	snv			1
rs7589342	NCK2			2	105817021	intron variant	C/T	snv		0.28	1
rs7589561	NCK2			2	105837629	intron variant	C/G;T	snv			1