DisGeNET - a database of gene-disease associations

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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 GENOME	Num. diseases
rs3784262	ALDH1A2	0.882	0.160	15	57960908	intron variant	T/A;C	snv		1
rs11635486	LOC283665 ; ALDH1A2			15	58068926	intron variant	G/A;C	snv		1
rs16953360	ALDH1A2 ; AQP9			15	58155995	non coding transcript exon variant	A/G	snv	2.3E-02	1
rs12441883	ALDH1A2 ; AQP9			15	58164651	intron variant	G/A	snv	0.12	1
rs16939881	ALDH1A2 ; AQP9			15	58179780	intron variant	G/C;T	snv		1
rs2077737	ALDH1A2			15	58186751	intron variant	T/C	snv	0.25	1
rs12900815	ALDH1A2			15	58193483	intron variant	C/G;T	snv		1
rs11857136	ALDH1A2			15	58208580	intron variant	T/A	snv	0.61	1
rs56227417	ALDH1A2			15	58208757	intron variant	T/C	snv	0.58	1
rs4350519	ALDH1A2			15	58208947	intron variant	C/G;T	snv		1
rs1618701	ALDH1A2			15	58209083	intron variant	T/A	snv	0.54	1
rs7180071	ALDH1A2			15	58210273	intron variant	A/G;T	snv		1
rs2414551	ALDH1A2			15	58210929	intron variant	T/C	snv	0.54	1
rs1663253	ALDH1A2			15	58212479	intron variant	C/T	snv	0.54	1
rs2017566	ALDH1A2			15	58212841	intron variant	T/C	snv	0.55	1
rs1663254	ALDH1A2			15	58221794	intron variant	G/A	snv	0.53	1
rs1663255	ALDH1A2			15	58222043	intron variant	C/T	snv	0.55	1
rs62000518	ALDH1A2			15	58253979	intron variant	T/C	snv	0.33	1
rs56314708	ALDH1A2			15	58254498	intron variant	C/A	snv	0.33	1
rs7183294	ALDH1A2			15	58254529	intron variant	T/C	snv	0.57	1
rs7182541	ALDH1A2			15	58254819	intron variant	C/A;T	snv		1
rs6493993	ALDH1A2			15	58255258	intron variant	T/C;G	snv		1
rs7173510	ALDH1A2			15	58257162	intron variant	C/T	snv	0.55	1
rs7179597	ALDH1A2			15	58257316	intron variant	T/G	snv	0.55	1
rs7179609	ALDH1A2			15	58257333	intron variant	T/C	snv	0.55	1