DisGeNET - a database of gene-disease associations

List of associated variants

Coinfection, C0275524

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
rs12979860	IFNL4	0.547	0.520	19	39248147	intron variant	C/T	snv		0.39	84
rs1801157	CXCL12	0.611	0.600	10	44372809	3 prime UTR variant	C/T	snv		0.16	46
rs3745274	CYP2B6	0.672	0.480	19	41006936	missense variant	G/A;T	snv	4.0E-06; 0.27		30
rs1127354	ITPA	0.667	0.400	20	3213196	missense variant	C/A;G	snv	7.5E-02		26
rs10774671	OAS1	0.732	0.480	12	112919388	splice acceptor variant	G/A;C	snv	0.67		14
rs7270101	ITPA	0.776	0.200	20	3213247	intron variant	A/C	snv	8.7E-02	9.7E-02	10
rs11003123	MBL2	0.827	0.200	10	52771774	upstream gene variant	G/A	snv		0.30	6
rs11003124	MBL2	1.000	0.040	10	52772131	upstream gene variant	T/G	snv		0.30	2
rs36014597	MBL2	1.000	0.080	10	52772040	upstream gene variant	T/C	snv		0.30	2
rs10824792	MBL2			10	52766446	3 prime UTR variant	C/T	snv		0.48	1
rs7084554	MBL2			10	52772053	upstream gene variant	T/C	snv		0.30	1