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
rs2893923	JMJD1C			10	63501424	intron variant	C/T	snv		0.27	1
rs143014767	JMJD1C			10	63304077	intron variant	CTTTGCC/-	del			1
rs2893919	MIR1296 ; JMJD1C			10	63375018	intron variant	G/A	snv		0.43	1
rs10822168	JMJD1C			10	63405424	intron variant	G/A	snv		0.43	1
rs10761750	JMJD1C			10	63368859	intron variant	G/A	snv		0.43	1
rs7896783	JMJD1C			10	63402393	intron variant	G/A;C	snv			1
rs7924036	JMJD1C			10	63431885	intron variant	G/A;T	snv			3
rs10822161	JMJD1C			10	63358443	intron variant	G/A;T	snv			1
rs10761739	JMJD1C			10	63302248	intron variant	G/C	snv		0.38	1
rs10740118	JMJD1C			10	63341447	intron variant	G/C	snv		0.38	1
rs10761741	JMJD1C	1.000	0.040	10	63306426	intron variant	G/T	snv		0.38	3
rs34524635	JMJD1C			10	63501417	intron variant	T/-	delins		0.43	1
rs10761733	JMJD1C			10	63275024	intron variant	T/A;C	snv			1
rs6479891	JMJD1C	1.000	0.120	10	63246696	intron variant	T/A;C	snv			1
rs7910927	JMJD1C			10	63379150	intron variant	T/A;G	snv			1
rs10995477	JMJD1C			10	63250912	intron variant	T/C	snv		0.43	4
rs4745706	JMJD1C			10	63399820	intron variant	T/C	snv		0.13	1
rs4379723	JMJD1C			10	63203689	intron variant	T/C	snv		0.43	1
rs41274072	JMJD1C			10	63214396	missense variant	T/C	snv	2.9E-02	5.3E-02	1
rs35997229	JMJD1C	1.000	0.080	10	63197831	intron variant	T/C;G	snv			1
rs7085862	JMJD1C			10	63486687	intron variant	T/G	snv		0.66	1
rs35632171	JMJD1C	1.000	0.080	10	63349742	intron variant	T/G	snv		2.8E-02	1
rs7088799	JMJD1C			10	63256414	intron variant	T/G	snv		0.38	1