DisGeNET - a database of gene-disease associations

List of associated variants

Pain, C0030193

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
rs138105638	CYP3A4			7	99766440	stop gained	G/A;T	snv	6.4E-05	7.7E-05	3
rs3845446	CACNA1E			1	181797301	intron variant	T/C	snv		6.3E-02	3
rs7016778	OPRK1			8	53237545	intron variant	A/T	snv		0.17	3
rs13080116	SCN11A			3	38865732	intron variant	T/C	snv		0.23	2
rs200207721	OPRM1			6	154039743	missense variant	A/G	snv	1.2E-05	1.4E-05	2
rs201059543	P2RX7 ; LOC105370032			12	121184366	missense variant	C/G;T	snv	4.0E-06; 3.6E-05		2
rs2817040	LOC285847 ; ARMC12			6	35737829	intron variant	G/A	snv		0.22	2
rs28362731	AQP1			7	30922175	missense variant	G/A	snv	3.1E-02	2.6E-02	2
rs33985936	SCN11A			3	38894643	missense variant	C/A;T	snv	8.0E-06; 0.22		2
rs3750625	ADRA2A			10	111079843	3 prime UTR variant	C/A	snv		8.7E-02	2
rs376128467	SCN11A			3	38894920	missense variant	A/G;T	snv	4.0E-06		2
rs3766246	FAAH			1	46399999	intron variant	A/C;G	snv			2
rs5993882	COMT			22	19950010	intron variant	T/C;G	snv			2
rs6473799	OPRK1			8	53240563	intron variant	A/G	snv		0.39	2
rs77114424	OPRM1			6	154039497	missense variant	G/A	snv			2
rs7734804	LOC105377703			5	164919530	intron variant	G/T	snv		8.3E-02	2
rs943552				1	156885826	downstream gene variant	C/T	snv		9.7E-02	2
rs9524885	ABCC4			13	95283335	intron variant	T/C	snv		0.63	2
rs11709492	SCN11A			3	38904493	intron variant	C/T	snv		0.26	1
rs11720013	SCN11A			3	38924745	intron variant	G/T	snv		1.0E-01	1
rs11720988	SCN11A			3	38865054	intron variant	G/A	snv		0.26	1
rs1172682117	ERG			21	38403690	synonymous variant	T/G	snv	4.0E-06		1
rs11898284	SCN1A-AS1 ; SCN9A			2	166325017	intron variant	A/G	snv		0.15	1
rs11988795	TRPA1 ; MSC-AS1			8	72037366	intron variant	C/G;T	snv			1
rs12478318	SCN1A-AS1 ; SCN9A			2	166277030	missense variant	T/G	snv	3.7E-02	1.3E-02	1