DisGeNET - a database of gene-disease associations

Source: ALL

Results per page

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
rs7827408	VPS13B			8	99527615	intron variant	C/T	snv		2.3E-02	3
rs11568746	TGFBR1			9	99105926	intron variant	C/G	snv		2.1E-05	6
rs4841132	LOC157273			8	9326086	non coding transcript exon variant	A/G	snv		0.89	14
rs9987289	LOC157273	1.000	0.040	8	9325848	non coding transcript exon variant	A/G	snv		0.87	10
rs2169387	LOC157273			8	9323885	intron variant	A/G	snv		0.87	6
rs4418728				10	93079967	downstream gene variant	G/T	snv		0.42	8
rs9658736	FAS			10	89004160	intron variant	T/C	snv		9.4E-03	3
rs16880248	CNR1			6	88141968	3 prime UTR variant	G/T	snv		2.7E-02	5
rs12258934	NRG3			10	82015079	intron variant	T/C	snv		5.1E-02	4
rs11574728	CD36			7	80676025	intron variant	G/A	snv		7.5E-03	3
rs4129767	PGS1			17	78407903	intron variant	G/A	snv		0.46	6
rs8071884	PGS1			17	78401977	intron variant	C/A;G;T	snv			4
rs4969183	PGS1			17	78397291	intron variant	A/G	snv		0.46	5
rs7939352	GAB2			11	78292105	intron variant	G/A	snv		0.27	4
rs4385188	CERT1			5	75438537	intron variant	A/G	snv		0.33	4
rs3846663	HMGCR ; CERT1	0.882	0.120	5	75359901	intron variant	C/T	snv		0.35	7
rs7703051		0.851	0.120	5	75329662	intron variant	C/A	snv		0.38	18
rs737410	ARRB1			11	75315038	intron variant	A/G	snv		4.3E-02	6
rs16957552	BCAR1			16	75235226	missense variant	T/C	snv	6.8E-03	2.8E-02	4
rs34604640	KCNE3			11	74457448	missense variant	G/C	snv	1.0E-04	1.3E-04	4
rs1874148	VCL			10	74114657	intron variant	A/G	snv		1.8E-02	6
rs17145738	TBL2	0.851	0.200	7	73568544	3 prime UTR variant	C/T	snv		0.11	11
rs34183407	ALMS1			2	73454052	missense variant	C/T	snv	2.1E-05	3.5E-05	6
rs3794695	HPR ; TXNL4B			16	72063928	intron variant	C/A;T	snv			4
rs760242	DHCR7			11	71435530	missense variant	C/T	snv	2.2E-04	6.3E-05	6