DisGeNET - a database of gene-disease associations

List of associated variants

Dizziness, C0012833

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
rs34637584	LRRK2	0.583	0.480	12	40340400	missense variant	G/A	snv	5.3E-04	3.6E-04	78
rs972936	IGF1 ; LINC02456	0.807	0.200	12	102431143	intron variant	T/C	snv		0.70	12
rs7136446	IGF1 ; LINC02456	0.882	0.160	12	102444737	intron variant	C/T	snv		0.66	8
rs3743077	CHRNA3	1.000	0.040	15	78602554	intron variant	C/T	snv		0.31	3
rs16979956	BMX ; ACE2			X	15525068	intron variant	C/T	snv		4.0E-04	2
rs35697037	BMX ; ACE2			X	15523993	intron variant	G/A	snv		0.37	2
rs2304297	CHRNA6			8	42753056	3 prime UTR variant	G/C	snv		0.39	2
rs7812298	CHRNA6			8	42753436	intron variant	C/T	snv		0.36	2
rs7828365	CHRNA6			8	42774171	intron variant	C/T	snv		0.14	2
rs7178176	CHRNA7			15	32151612	intron variant	C/T	snv		0.18	2
rs755204	LOC100130587 ; CHRNA4			20	63362813	intron variant	G/A	snv		8.6E-02	2