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
rs17821298	ALDH1A2			15	58398539	intron variant	C/A;T	snv		1
rs17821274	ALDH1A2			15	58392279	intron variant	T/C	snv	0.55	1
rs1663255	ALDH1A2			15	58222043	intron variant	C/T	snv	0.55	1
rs2077737	ALDH1A2			15	58186751	intron variant	T/C	snv	0.25	1
rs1663253	ALDH1A2			15	58212479	intron variant	C/T	snv	0.54	1
rs17821268	ALDH1A2			15	58359098	intron variant	T/C	snv	0.32	1
rs7350789	ALDH1A2			15	58387469	intron variant	G/A	snv	0.35	1
rs12904030	ALDH1A2			15	58270071	intron variant	C/G;T	snv	0.57	1
rs17821159	ALDH1A2			15	58264863	intron variant	A/G	snv	0.32	1
rs7178337	ALDH1A2			15	58257413	intron variant	A/C	snv	0.55	1
rs6493993	ALDH1A2			15	58255258	intron variant	T/C;G	snv		1
rs11858759	ALDH1A2			15	58384622	intron variant	G/A	snv	0.23	1
rs12903590	ALDH1A2			15	58285578	intron variant	A/T	snv	0.15	1
rs4622454	ALDH1A2			15	58354133	intron variant	C/G;T	snv		1
rs11858481	ALDH1A2			15	58396998	intron variant	C/T	snv	0.20	1
rs1663254	ALDH1A2			15	58221794	intron variant	G/A	snv	0.53	1
rs1444942	ALDH1A2			15	58393614	intron variant	G/A;C	snv		1
rs2414578	ALDH1A2			15	58388440	intron variant	T/C	snv	0.40	1
rs12905732	ALDH1A2			15	58391343	intron variant	G/C	snv	0.15	1
rs8037464	ALDH1A2			15	58357278	intron variant	T/C	snv	0.24	1
rs7497636	ALDH1A2			15	58393432	intron variant	C/T	snv	0.13	1
rs17240869	ALDH1A2			15	58408112	intron variant	T/C	snv	0.17	1
rs2414577	ALDH1A2			15	58388439	intron variant	T/C	snv	0.40	1
rs723967	ALDH1A2			15	58404101	intron variant	T/C	snv	0.40	1