DisGeNET - a database of gene-disease associations

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Variants associated to the Gene: IGF1 ×

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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
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
rs5742663	IGF1 ; LINC02456			12	102430212	intron variant	T/A;G	snv			1
rs972936	IGF1 ; LINC02456	0.807	0.200	12	102431143	intron variant	T/C	snv		0.70	12
rs5742626	LINC02456 ; IGF1			12	102464131	intron variant	T/C	snv		2.3E-02	3
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
rs978458	IGF1 ; LINC02456	0.925	0.120	12	102408461	intron variant	T/C	snv		0.69	2
rs5742629	LINC02456 ; IGF1	1.000	0.040	12	102463485	non coding transcript exon variant	T/C	snv		0.32	1
rs5742643	LINC02456 ; IGF1			12	102444085	intron variant	T/C	snv		0.76	1
rs7300373	IGF1 ; LINC02456			12	102438008	intron variant	T/G	snv		1.4E-02	1