DisGeNET - a database of gene-disease associations

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Variants associated to the Gene: IGF1 ×

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Gene

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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
rs5742617	IGF1			12	102476127	intron variant	C/T	snv		8.7E-03	1
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
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
rs587779350	LINC02456 ; IGF1	1.000	0.120	12	102419619	missense variant	G/A	snv		7.0E-06	1
rs7300373	IGF1 ; LINC02456			12	102438008	intron variant	T/G	snv		1.4E-02	1
rs748799635	IGF1	1.000	0.080	12	102475727	missense variant	C/T	snv	8.0E-06		1
rs749124997	LINC02456 ; HELLPAR ; IGF1	1.000	0.040	12	102402539	missense variant	C/T	snv	4.0E-06		1
rs776234219	IGF1 ; LINC02456	1.000	0.040	12	102419531	missense variant	G/A	snv	1.6E-05	3.5E-05	1
rs9308315	LINC02456 ; IGF1			12	102410115	intron variant	A/C;T	snv			1