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
rs10761731	JMJD1C			10	63267850	intron variant	A/T	snv	0.38	6
rs7896518	JMJD1C			10	63344740	intron variant	A/G	snv	0.38	4
rs10995477	JMJD1C			10	63250912	intron variant	T/C	snv	0.43	4
rs7916868	JMJD1C			10	63229171	intron variant	A/T	snv	0.47	3
rs7924036	JMJD1C			10	63431885	intron variant	G/A;T	snv		3
rs10761741	JMJD1C	1.000	0.040	10	63306426	intron variant	G/T	snv	0.38	3
rs2393967	MIR1296 ; JMJD1C			10	63373396	intron variant	A/C	snv	0.23	3
rs7899503	JMJD1C			10	63327708	intron variant	C/G;T	snv		2
rs7082066	JMJD1C			10	63239211	intron variant	A/G	snv	0.69	2
rs3999089	JMJD1C			10	63444048	intron variant	A/G	snv	0.41	2
rs7902343	JMJD1C			10	63245639	intron variant	C/T	snv	0.40	2
rs75446656	JMJD1C	1.000	0.080	10	63340256	intron variant	C/A;T	snv		1
rs10761739	JMJD1C			10	63302248	intron variant	G/C	snv	0.38	1
rs10761733	JMJD1C			10	63275024	intron variant	T/A;C	snv		1
rs10995505	JMJD1C			10	63331399	intron variant	A/G;T	snv		1
rs6479901	JMJD1C			10	63421016	intron variant	C/A	snv	0.66	1
rs4745706	JMJD1C			10	63399820	intron variant	T/C	snv	0.13	1
rs10761751	JMJD1C			10	63395125	intron variant	A/G	snv	0.42	1
rs4379723	JMJD1C			10	63203689	intron variant	T/C	snv	0.43	1
rs7085862	JMJD1C			10	63486687	intron variant	T/G	snv	0.66	1
rs7075195	JMJD1C			10	63290899	intron variant	A/G	snv	0.38	1
rs12355784	JMJD1C			10	63361805	intron variant	C/A;T	snv		1
rs10761779	JMJD1C			10	63515167	intron variant	A/G	snv	0.42	1
rs10822161	JMJD1C			10	63358443	intron variant	G/A;T	snv		1
rs7910927	JMJD1C			10	63379150	intron variant	T/A;G	snv		1