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
rs7136446	IGF1 ; LINC02456	0.882	0.160	12	102444737	intron variant	C/T	snv		0.66	8
rs7300373	IGF1 ; LINC02456			12	102438008	intron variant	T/G	snv		1.4E-02	1
rs745410279	IGF1	0.925	0.200	12	102478498	missense variant	T/C	snv	4.1E-06		2
rs745805222	IGF1	0.790	0.120	12	102475722	synonymous variant	C/T	snv	1.2E-05	4.9E-05	7
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
rs7956547	IGF1	0.925	0.120	12	102465038	intron variant	T/C	snv		0.25	2
rs9308315	LINC02456 ; IGF1			12	102410115	intron variant	A/C;T	snv			1
rs972936	IGF1 ; LINC02456	0.807	0.200	12	102431143	intron variant	T/C	snv		0.70	12
rs978458	IGF1 ; LINC02456	0.925	0.120	12	102408461	intron variant	T/C	snv		0.69	2