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 EXOME	AF GENOME	Num. diseases
rs2393967	MIR1296 ; JMJD1C			10	63373396	intron variant	A/C	snv		0.23	3
rs7896518	JMJD1C			10	63344740	intron variant	A/G	snv		0.38	4
rs7082066	JMJD1C			10	63239211	intron variant	A/G	snv		0.69	2
rs3999089	JMJD1C			10	63444048	intron variant	A/G	snv		0.41	2
rs10761751	JMJD1C			10	63395125	intron variant	A/G	snv		0.42	1
rs7075195	JMJD1C			10	63290899	intron variant	A/G	snv		0.38	1
rs7923609	MIR1296 ; JMJD1C			10	63374062	intron variant	A/G	snv		0.43	1
rs10761779	JMJD1C			10	63515167	intron variant	A/G	snv		0.42	1
rs9415676	JMJD1C			10	63250866	intron variant	A/G	snv		0.44	1
rs10761765	JMJD1C ; LOC105378330			10	63429213	intron variant	A/G;T	snv			1
rs10995505	JMJD1C			10	63331399	intron variant	A/G;T	snv			1
rs10740128	JMJD1C			10	63490783	intron variant	A/G;T	snv			1
rs10761731	JMJD1C			10	63267850	intron variant	A/T	snv		0.38	6
rs7916868	JMJD1C			10	63229171	intron variant	A/T	snv		0.47	3
rs6479901	JMJD1C			10	63421016	intron variant	C/A	snv		0.66	1
rs7080386	JMJD1C			10	63288546	intron variant	C/A	snv		0.38	1
rs1935	JMJD1C			10	63168063	missense variant	C/A;G;T	snv	4.0E-06; 0.44		1
rs75446656	JMJD1C	1.000	0.080	10	63340256	intron variant	C/A;T	snv			1
rs12355784	JMJD1C			10	63361805	intron variant	C/A;T	snv			1
rs34044188	JMJD1C	1.000	0.080	10	63497603	intron variant	C/A;T	snv			1
rs7899503	JMJD1C			10	63327708	intron variant	C/G;T	snv			2
rs7902343	JMJD1C			10	63245639	intron variant	C/T	snv		0.40	2
rs10822145	JMJD1C			10	63174788	intron variant	C/T	snv		0.44	1
rs4454603	JMJD1C			10	63252990	intron variant	C/T	snv		0.43	1
rs10761756	JMJD1C			10	63412568	intron variant	C/T	snv		0.42	1