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 GENOME	Num. diseases
rs3736802	TRPC4AP	1.000	0.080	20	35016239	intron variant	T/C	snv	0.53	3
rs1885119	TRPC4AP	1.000	0.080	20	35057846	intron variant	T/C	snv	0.58	3
rs6088692	TRPC4AP	1.000	0.080	20	35050785	intron variant	A/G	snv	0.58	3
rs6120816	TRPC4AP	1.000	0.080	20	35056555	intron variant	G/A;C	snv		3
rs6087664	TRPC4AP	1.000	0.080	20	35038413	intron variant	C/A;G;T	snv		3
rs3818253	TRPC4AP	1.000	0.040	20	35009073	intron variant	G/A	snv	0.19	3
rs2889873	TRPC4AP			20	35059038	intron variant	G/A	snv	8.2E-02	2
rs6119560	TRPC4AP			20	35019174	intron variant	G/C	snv	0.19	2
rs1885117	TRPC4AP			20	35012937	intron variant	C/T	snv	0.18	2
rs7263253	TRPC4AP			20	35061573	intron variant	T/A;C	snv		2
rs6120828	TRPC4AP			20	35086657	intron variant	T/C	snv	0.18	2
rs6120790	TRPC4AP			20	35011287	intron variant	A/T	snv	0.19	2
rs2145557	TRPC4AP			20	35079757	intron variant	A/G	snv	0.58	2
rs4911460	TRPC4AP			20	35036527	intron variant	G/A;C	snv	0.58	2
rs6120797	TRPC4AP			20	35018199	intron variant	G/A	snv	0.19	2
rs6088687	TRPC4AP			20	35036947	intron variant	G/A	snv	0.58	2
rs3803937	TRPC4AP			20	35044884	intron variant	C/A;T	snv		2
rs6088690	TRPC4AP			20	35045523	intron variant	A/G	snv	0.19	2
rs7273734	TRPC4AP			20	35011600	intron variant	G/A;C	snv		2
rs2378332	TRPC4AP			20	35029447	intron variant	A/C;G;T	snv		2
rs6088691	TRPC4AP			20	35045955	intron variant	C/T	snv	0.18	2
rs6120804	TRPC4AP			20	35035898	intron variant	C/A	snv	0.19	2
rs6120812	TRPC4AP			20	35041624	intron variant	T/C	snv	0.18	2
rs6087660	TRPC4AP			20	35028725	intron variant	T/C	snv	0.59	2
rs7271729	TRPC4AP			20	35023189	intron variant	C/T	snv	8.0E-02	2