DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: ZPBP2 ×

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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
rs12150079	ZPBP2	0.807	0.280	17	39869164	intron variant	G/A	snv		0.24	9
rs35736272	ZPBP2	0.807	0.160	17	39876427	intron variant	T/C	snv		0.35	6
rs11557467	ZPBP2	0.851	0.200	17	39872381	missense variant	G/T	snv	0.45	0.45	5
rs4795397	ZPBP2	0.925	0.160	17	39867492	upstream gene variant	A/G	snv		0.38	4
rs10852936	ZPBP2	0.925	0.120	17	39875461	intron variant	C/T	snv	0.39	0.40	3
rs11078925	ZPBP2	0.925	0.160	17	39868955	intron variant	T/C	snv		0.36	3
rs11557466	ZPBP2	0.925	0.160	17	39868373	synonymous variant	C/T	snv	0.40	0.36	3
rs11870965	ZPBP2	0.925	0.160	17	39873952	intron variant	T/A	snv		0.40	3
rs12936231	ZPBP2	0.925	0.160	17	39872867	intron variant	C/G;T	snv			3
rs1054609	ZPBP2	0.925	0.160	17	39877024	3 prime UTR variant	A/C	snv		0.40	2
rs10852935	ZPBP2	1.000	0.080	17	39875421	synonymous variant	C/T	snv	0.40	0.35	1
rs11650661	ZPBP2	1.000	0.080	17	39870033	intron variant	A/C;T	snv			1
rs11655198	ZPBP2	1.000	0.080	17	39869916	intron variant	C/T	snv		0.43	1
rs11658278	ZPBP2	1.000	0.080	17	39874911	intron variant	T/C	snv		0.46	1
rs12709365	ZPBP2	1.000	0.080	17	39871147	intron variant	A/G	snv		0.40	1
rs12939457	ZPBP2	1.000	0.120	17	39875935	intron variant	T/C	snv		0.38	1
rs13380815	ZPBP2	1.000	0.080	17	39871330	intron variant	A/G	snv		0.40	1
rs189660050	ZPBP2	1.000	0.040	17	39870781	missense variant	C/T	snv	2.8E-05	1.9E-04	1
rs34189114	ZPBP2	1.000	0.080	17	39876207	intron variant	C/T	snv		0.36	1
rs36095411	ZPBP2	1.000	0.080	17	39875612	intron variant	T/A;G	snv			1
rs59716545	ZPBP2	1.000	0.120	17	39875604	intron variant	T/G	snv		0.35	1
rs9891174	ZPBP2	1.000	0.080	17	39875549	intron variant	T/A	snv		0.39	1
rs9903250	ZPBP2	1.000	0.080	17	39874777	intron variant	G/A	snv		0.43	1