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
rs978458	IGF1 ; LINC02456	0.925	0.120	12	102408461	intron variant	T/C	snv		0.69	2
rs972936	IGF1 ; LINC02456	0.807	0.200	12	102431143	intron variant	T/C	snv		0.70	12
rs9308315	LINC02456 ; IGF1			12	102410115	intron variant	A/C;T	snv			1
rs7956547	IGF1	0.925	0.120	12	102465038	intron variant	T/C	snv		0.25	2
rs776234219	IGF1 ; LINC02456	1.000	0.040	12	102419531	missense variant	G/A	snv	1.6E-05	3.5E-05	1
rs749124997	LINC02456 ; HELLPAR ; IGF1	1.000	0.040	12	102402539	missense variant	C/T	snv	4.0E-06		1
rs748799635	IGF1	1.000	0.080	12	102475727	missense variant	C/T	snv	8.0E-06		1
rs745805222	IGF1	0.790	0.120	12	102475722	synonymous variant	C/T	snv	1.2E-05	4.9E-05	7
rs745410279	IGF1	0.925	0.200	12	102478498	missense variant	T/C	snv	4.1E-06		2
rs7300373	IGF1 ; LINC02456			12	102438008	intron variant	T/G	snv		1.4E-02	1
rs7136446	IGF1 ; LINC02456	0.882	0.160	12	102444737	intron variant	C/T	snv		0.66	8
rs6220	LINC02456 ; HELLPAR ; IGF1	0.925	0.080	12	102400737	3 prime UTR variant	G/A	snv		0.67	4
rs6219	HELLPAR ; LINC02456 ; IGF1	1.000	0.080	12	102396414	3 prime UTR variant	C/T	snv		8.9E-02	2
rs6218	LINC02456 ; HELLPAR ; IGF1	0.732	0.440	12	102399855	3 prime UTR variant	A/G	snv		2.1E-02	13
rs6214	LINC02456 ; HELLPAR ; IGF1	0.672	0.400	12	102399791	3 prime UTR variant	C/T	snv		0.45	26
rs587779350	LINC02456 ; IGF1	1.000	0.120	12	102419619	missense variant	G/A	snv		7.0E-06	1
rs5742714	IGF1 ; HELLPAR ; LINC02456	0.882	0.160	12	102396074	3 prime UTR variant	C/G	snv		8.9E-02	3
rs5742692	LINC02456 ; IGF1			12	102405820	intron variant	A/G	snv		6.6E-02	2
rs5742683	LINC02456 ; IGF1			12	102419939	intron variant	A/G	snv		3.3E-02	1
rs5742663	IGF1 ; LINC02456			12	102430212	intron variant	T/A;G	snv			1
rs5742643	LINC02456 ; IGF1			12	102444085	intron variant	T/C	snv		0.76	1
rs5742632	LINC02456 ; IGF1	0.851	0.120	12	102462696	intron variant	A/G	snv		0.26	4
rs5742629	LINC02456 ; IGF1	1.000	0.040	12	102463485	non coding transcript exon variant	T/C	snv		0.32	1
rs5742626	LINC02456 ; IGF1			12	102464131	intron variant	T/C	snv		2.3E-02	3
rs5742617	IGF1			12	102476127	intron variant	C/T	snv		8.7E-03	1