DisGeNET - a database of gene-disease associations

List of associated variants

Withdrawal Symptoms, C0087169

Source: ALL

Results per page

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
rs7439366	UGT2B7	0.752	0.320	4	69098620	missense variant	T/C	snv	0.56	0.57	16
rs2066702	ADH1B	0.882	0.080	4	99307860	missense variant	G/A	snv	1.5E-02	5.9E-02	7
rs2242480	CYP3A4	0.882	0.120	7	99763843	intron variant	C/T	snv	0.22	0.32	5
rs12675595				8	53255365	upstream gene variant	G/A	snv		6.2E-02	3
rs752949	SLC1A2	0.925	0.160	11	35306201	synonymous variant	C/T	snv	0.23	0.22	3
rs3762894	ADH4 ; LOC100507053	1.000	0.080	4	99144933	intron variant	T/C	snv		0.19	2
rs4646440	CYP3A4			7	99763247	intron variant	G/A	snv		5.1E-02	2
rs4292394	UGT2B7			4	69107231	synonymous variant	C/G	snv	0.56	0.59	2
rs6600893	UGT2B7			4	69113183	downstream gene variant	T/C	snv		0.59	2
rs8192475	CHRNA3			15	78618888	missense variant	C/G;T	snv	2.9E-02		1