DisGeNET - a database of gene-disease associations

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Variants associated to the Gene: IGF1 ×

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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
rs121912430	LINC02456 ; IGF1	1.000	0.120	12	102419637	missense variant	C/T	snv		1
rs1239905891	IGF1	0.925	0.080	12	102475786	missense variant	G/A;T	snv		3
rs12423791	IGF1	0.925	0.040	12	102465050	intron variant	G/C	snv	2.8E-02	5
rs1520220	LINC02456 ; IGF1	0.807	0.280	12	102402744	intron variant	G/C;T	snv	0.76	9
rs2072592	IGF1 ; LINC02456	0.925	0.120	12	102419854	intron variant	C/T	snv	2.8E-02	2
rs2162679	IGF1	0.851	0.240	12	102477481	intron variant	C/G;T	snv		6
rs2195239	LINC02456 ; IGF1	0.851	0.240	12	102462924	non coding transcript exon variant	C/G	snv	0.28	7
rs2288377	LOC105369944 ; IGF1	0.925	0.080	12	102480984	intron variant	A/G;T	snv		2
rs35767	IGF1 ; LOC105369944	0.763	0.360	12	102481791	upstream gene variant	A/C;G;T	snv		13
rs4764887	IGF1 ; LINC02456	0.925	0.080	12	102430122	intron variant	G/A	snv	2.2E-02	2
rs5742612	LOC105369944 ; IGF1	0.752	0.440	12	102481086	intron variant	A/G	snv	5.6E-02	11
rs5742617	IGF1			12	102476127	intron variant	C/T	snv	8.7E-03	1
rs5742626	LINC02456 ; IGF1			12	102464131	intron variant	T/C	snv	2.3E-02	3
rs5742629	LINC02456 ; IGF1	1.000	0.040	12	102463485	non coding transcript exon variant	T/C	snv	0.32	1
rs5742632	LINC02456 ; IGF1	0.851	0.120	12	102462696	intron variant	A/G	snv	0.26	4
rs5742643	LINC02456 ; IGF1			12	102444085	intron variant	T/C	snv	0.76	1
rs5742663	IGF1 ; LINC02456			12	102430212	intron variant	T/A;G	snv		1
rs5742683	LINC02456 ; IGF1			12	102419939	intron variant	A/G	snv	3.3E-02	1
rs5742692	LINC02456 ; IGF1			12	102405820	intron variant	A/G	snv	6.6E-02	2
rs5742714	IGF1 ; HELLPAR ; LINC02456	0.882	0.160	12	102396074	3 prime UTR variant	C/G	snv	8.9E-02	3
rs587779350	LINC02456 ; IGF1	1.000	0.120	12	102419619	missense variant	G/A	snv	7.0E-06	1
rs6214	LINC02456 ; HELLPAR ; IGF1	0.672	0.400	12	102399791	3 prime UTR variant	C/T	snv	0.45	26
rs6218	LINC02456 ; HELLPAR ; IGF1	0.732	0.440	12	102399855	3 prime UTR variant	A/G	snv	2.1E-02	13
rs6219	HELLPAR ; LINC02456 ; IGF1	1.000	0.080	12	102396414	3 prime UTR variant	C/T	snv	8.9E-02	2
rs6220	LINC02456 ; HELLPAR ; IGF1	0.925	0.080	12	102400737	3 prime UTR variant	G/A	snv	0.67	4