DisGeNET - a database of gene-disease associations

List of associated variants

Postoperative Nausea and Vomiting, C0520909

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
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs2032582	ABCB1	0.538	0.800	7	87531302	missense variant	A/C;T	snv	0.54; 3.8E-02		97
rs1799971	OPRM1	0.559	0.600	6	154039662	missense variant	A/G	snv	0.19	0.12	95
rs1800497	ANKK1	0.620	0.400	11	113400106	missense variant	G/A	snv	0.26	0.26	56
rs324420	FAAH	0.637	0.440	1	46405089	missense variant	C/A	snv	0.24	0.26	48
rs1176744	HTR3B	0.708	0.240	11	113932306	missense variant	A/C	snv	0.33	0.36	19
rs4795541	SLC6A4 ; LOC105371720	0.807	0.200	17	30237299	upstream gene variant	A/G	snv			7
rs12208357	SLC22A1	1.000	0.080	6	160122116	missense variant	C/T	snv	5.2E-02	4.9E-02	5
rs349358	KCNB2			8	72539240	intron variant	C/T	snv		0.88	3
rs510769	OPRM1	1.000	0.080	6	154040884	intron variant	C/T	snv		0.25	2
rs2165870	LOC105373225 ; CHRM3			1	239622120	intron variant	A/C;G	snv		0.75	1
rs1323042	OPRM1			6	154100709	intron variant	G/T	snv		0.49	1
rs3798683	OPRM1			6	154097279	intron variant	G/A	snv		0.15	1
rs4870266	OPRM1			6	154047863	intron variant	G/A	snv		5.5E-02	1
rs609623	OPRM1			6	154103824	intron variant	T/A;C	snv			1
rs644261	OPRM1			6	154121116	3 prime UTR variant	G/A;C;T	snv			1
rs9397685	OPRM1			6	154112099	intron variant	A/G	snv		6.7E-03	1
rs3755468	TACR1 ; LOC105374811 ; LOC105374812			2	75155265	intron variant	T/C	snv		0.59	1