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
rs8089865	DCC	1.000	0.040	18	53431552	intron variant	G/A;C	snv			4
rs1431196	DCC	1.000	0.040	18	53305732	intron variant	A/G	snv	0.31	0.30	2
rs4277413	DCC	1.000	0.040	18	53172556	intron variant	G/A;C	snv			2
rs10221412	DCC			18	53198102	intron variant	T/A;C	snv			1
rs10502966	DCC			18	53222129	intron variant	A/G;T	snv			1
rs1078459	DCC			18	53249921	intron variant	T/A;C;G	snv			1
rs10853627	DCC			18	53179703	intron variant	T/A;C	snv			1
rs11662271	DCC			18	53380995	intron variant	T/C	snv		0.46	1
rs11663156	DCC			18	53385388	intron variant	T/C	snv		0.27	1
rs11665242	DCC			18	53380757	intron variant	A/G	snv		0.30	1
rs12607356	DCC			18	52917911	intron variant	G/A	snv		0.39	1
rs12960505	DCC			18	53445812	intron variant	G/T	snv		0.47	1
rs13381096	DCC			18	53423032	intron variant	C/A	snv		0.31	1
rs1367633	DCC			18	53221586	intron variant	G/A	snv		0.36	1
rs1502233	DCC			18	53464065	intron variant	T/C	snv		0.58	1
rs17411061	DCC			18	53268743	intron variant	C/T	snv		0.30	1
rs17417046	DCC			18	53458627	intron variant	C/T	snv		0.33	1
rs1972044	DCC			18	53404710	intron variant	G/A	snv		0.32	1
rs62100775	DCC			18	53227723	intron variant	A/G	snv		0.30	1
rs6508220	DCC			18	53304806	intron variant	A/G	snv		0.58	1
rs71367283	DCC			18	52525714	intron variant	A/C	snv		2.1E-02	1
rs7245004	DCC			18	53190575	intron variant	C/A;G	snv			1
rs7506451	DCC			18	53044061	intron variant	T/A	snv		0.33	1
rs8083850	DCC			18	53180922	intron variant	A/G	snv		0.35	1
rs9949444	DCC			18	53169534	intron variant	A/C	snv		0.38	1