DisGeNET - a database of gene-disease associations

List of shared variants

C-reactive protein measurement, C0201657

Disease: Fibrinogen, CTCAE

Source: ALL

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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
rs2228145	IL6R	0.602	0.720	1	154454494	missense variant	A/C;T	snv	0.38; 1.2E-05		57
rs4129267	IL6R	0.807	0.200	1	154453788	intron variant	C/G;T	snv			13
rs4537545	IL6R	0.790	0.160	1	154446403	intron variant	C/T	snv		0.48	11
rs12239046	NLRP3			1	247438293	intron variant	T/C	snv		0.58	9
rs6734238		1.000	0.080	2	113083453	upstream gene variant	A/G	snv		0.39	8
rs7529229	IL6R	0.851	0.120	1	154448302	intron variant	T/C	snv		0.48	8
rs10512597	RAB37 ; CD300LF			17	74703694	intron variant	T/A;C	snv			4
rs7518199	IL6R			1	154434943	intron variant	A/C;T	snv	0.39; 4.2E-06		4