DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: ARHGAP15 ×

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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
rs2034604	ARHGAP15	0.776	0.160	2	143201176	intron variant	C/G;T	snv		8
rs74847330	ARHGAP15			2	143074030	intergenic variant	A/G	snv	8.8E-02	4
rs35825582	ARHGAP15	1.000	0.040	2	143491193	intron variant	G/A	snv	0.45	3
rs79716587	ARHGAP15			2	143129250	intron variant	G/A	snv	7.9E-02	3
rs4662344	ARHGAP15	0.925	0.080	2	143591289	intron variant	T/C	snv	0.82	2
rs13428598	ARHGAP15			2	143492918	intron variant	C/T	snv	0.28	2
rs4273169	ARHGAP15	1.000	0.040	2	143473740	intron variant	G/A;C	snv		2
rs13413953	ARHGAP15	1.000	0.040	2	143479467	intron variant	T/G	snv	0.25	2
rs34030812	ARHGAP15	1.000	0.040	2	143491336	intron variant	T/C	snv	0.29	2
rs73962318	MTND4P22 ; ARHGAP15			2	143097365	non coding transcript exon variant	T/C	snv	4.2E-02	2
rs35125029	ARHGAP15			2	143504088	intron variant	G/A	snv	0.26	1
rs16858573	ARHGAP15	1.000	0.040	2	143118156	intron variant	T/C	snv	8.7E-02	1
rs4233567	ARHGAP15			2	143514807	intron variant	C/T	snv	0.25	1
rs10191758	ARHGAP15			2	143505711	intron variant	A/G	snv	0.30	1
rs10200533	ARHGAP15			2	143425433	intron variant	G/A	snv	0.54	1
rs10204230	ARHGAP15			2	143512879	intron variant	T/C	snv	0.42	1
rs12465778	ARHGAP15			2	143497632	intron variant	T/C	snv	0.46	1
rs10189912	ARHGAP15			2	143405040	intron variant	A/G	snv	0.27	1
rs62172064	ARHGAP15			2	143397319	intron variant	T/C	snv	1.2E-02	1
rs141234028	ARHGAP15			2	143570965	intron variant	C/T	snv	7.7E-03	1
rs140397066	ARHGAP15			2	143404536	intron variant	A/G	snv	3.1E-03	1
rs7606205	ARHGAP15			2	143388742	intron variant	A/C	snv	0.36	1
rs12991555	ARHGAP15			2	143429947	intron variant	A/G;T	snv		1
rs6710871	ARHGAP15			2	143203024	intron variant	G/A	snv	0.17	1
rs13002158	ARHGAP15			2	143264143	intron variant	A/G	snv	0.22	1