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 EXOME	AF GENOME	Num. diseases
rs6214	LINC02456 ; HELLPAR ; IGF1	0.672	0.400	12	102399791	3 prime UTR variant	C/T	snv		0.45	26
rs35767	IGF1 ; LOC105369944	0.763	0.360	12	102481791	upstream gene variant	A/C;G;T	snv			13
rs6218	LINC02456 ; HELLPAR ; IGF1	0.732	0.440	12	102399855	3 prime UTR variant	A/G	snv		2.1E-02	13
rs972936	IGF1 ; LINC02456	0.807	0.200	12	102431143	intron variant	T/C	snv		0.70	12
rs5742612	LOC105369944 ; IGF1	0.752	0.440	12	102481086	intron variant	A/G	snv		5.6E-02	11
rs1520220	LINC02456 ; IGF1	0.807	0.280	12	102402744	intron variant	G/C;T	snv		0.76	9
rs7136446	IGF1 ; LINC02456	0.882	0.160	12	102444737	intron variant	C/T	snv		0.66	8
rs745805222	IGF1	0.790	0.120	12	102475722	synonymous variant	C/T	snv	1.2E-05	4.9E-05	7
rs2195239	LINC02456 ; IGF1	0.851	0.240	12	102462924	non coding transcript exon variant	C/G	snv		0.28	7
rs2162679	IGF1	0.851	0.240	12	102477481	intron variant	C/G;T	snv			6
rs12423791	IGF1	0.925	0.040	12	102465050	intron variant	G/C	snv		2.8E-02	5
rs6220	LINC02456 ; HELLPAR ; IGF1	0.925	0.080	12	102400737	3 prime UTR variant	G/A	snv		0.67	4
rs5742632	LINC02456 ; IGF1	0.851	0.120	12	102462696	intron variant	A/G	snv		0.26	4
rs1239905891	IGF1	0.925	0.080	12	102475786	missense variant	G/A;T	snv			3
rs5742714	IGF1 ; HELLPAR ; LINC02456	0.882	0.160	12	102396074	3 prime UTR variant	C/G	snv		8.9E-02	3
rs5742626	LINC02456 ; IGF1			12	102464131	intron variant	T/C	snv		2.3E-02	3
rs6219	HELLPAR ; LINC02456 ; IGF1	1.000	0.080	12	102396414	3 prime UTR variant	C/T	snv		8.9E-02	2
rs745410279	IGF1	0.925	0.200	12	102478498	missense variant	T/C	snv	4.1E-06		2
rs7956547	IGF1	0.925	0.120	12	102465038	intron variant	T/C	snv		0.25	2
rs2072592	IGF1 ; LINC02456	0.925	0.120	12	102419854	intron variant	C/T	snv		2.8E-02	2
rs4764887	IGF1 ; LINC02456	0.925	0.080	12	102430122	intron variant	G/A	snv		2.2E-02	2
rs978458	IGF1 ; LINC02456	0.925	0.120	12	102408461	intron variant	T/C	snv		0.69	2
rs5742692	LINC02456 ; IGF1			12	102405820	intron variant	A/G	snv		6.6E-02	2
rs2288377	LOC105369944 ; IGF1	0.925	0.080	12	102480984	intron variant	A/G;T	snv			2
rs5742617	IGF1			12	102476127	intron variant	C/T	snv		8.7E-03	1