DisGeNET - a database of gene-disease associations

List of associated variants

High density lipoprotein measurement, C0392885

Source: GWASCAT ×

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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
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	35
rs2075290	ZPR1	0.882	0.160	11	116782580	intron variant	C/G;T	snv			5
rs6589566	ZPR1	0.882	0.080	11	116781707	intron variant	G/A;C;T	snv			5
rs11604424	ZPR1			11	116780399	intron variant	C/G;T	snv			3
rs12286037	ZPR1	1.000	0.040	11	116781491	intron variant	C/T	snv		0.11	3
rs2160669	ZPR1	1.000	0.040	11	116776891	3 prime UTR variant	C/T	snv		0.92	3
rs3741298	ZPR1			11	116786845	intron variant	C/T	snv		0.73	3
rs3741297	ZPR1			11	116786951	intron variant	C/T	snv	8.6E-03	1.0E-02	1
rs7483863	ZPR1			11	116781775	intron variant	A/G	snv		0.93	1
rs8142788	ZNRF3			22	29004527	intron variant	G/A	snv		0.11	1
rs7307277	ZNF664 ; RFLNA ; ZNF664-RFLNA			12	123990609	intron variant	A/G	snv		0.32	2
rs863750	ZNF664-RFLNA ; RFLNA			12	124020897	intron variant	C/T	snv		0.53	7
rs11652146	ZNF652			17	49345001	intron variant	G/A;C	snv			4
rs4805755	ZNF507			19	32363564	intron variant	C/T	snv		0.19	4
rs4465830	ZNF335			20	45956781	intron variant	A/G	snv		0.13	3
rs6073972	ZNF335			20	45961659	non coding transcript exon variant	C/G	snv		0.13	2
rs6124760	ZNF335			20	45952814	intron variant	C/G	snv		4.7E-02	1
rs7190256	ZFHX3	0.851	0.120	16	72963084	intron variant	C/T	snv		0.94	16
rs12369179	ZCCHC8	0.851	0.120	12	122479003	intron variant	C/T	snv		5.9E-02	16
rs10408163	ZC3H4			19	47093845	non coding transcript exon variant	T/C	snv		0.52	6
rs2303108	ZC3H4			19	47086638	intron variant	T/C	snv		0.63	3
rs661171	ZC3H12C ; RDX			11	110145794	intron variant	T/G	snv		0.69	5
rs10789752	ZC3H12C ; RDX			11	110109220	intron variant	T/A;C	snv			1
rs689183	ZC3H12C ; RDX			11	110141418	intron variant	G/T	snv		0.74	1
rs746463	ZC3H12C ; RDX			11	110125219	intron variant	C/T	snv		0.71	1