DisGeNET - a database of gene-disease associations

List of associated variants

Calcification of coronary artery, C1611184

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 GENOME	Num. diseases
rs10811643	CDKN2B-AS1	1.000	0.040	9	22024967	intron variant	A/G	snv	0.56	2
rs10811645	CDKN2B-AS1	1.000	0.040	9	22049657	intron variant	G/A	snv	0.59	2
rs10811651	CDKN2B-AS1	1.000	0.040	9	22067831	intron variant	G/A;C	snv		2
rs10965224	CDKN2B-AS1	1.000	0.040	9	22067277	intron variant	T/A	snv	0.64	2
rs113533135	LRP1B	1.000	0.080	2	140268867	intron variant	T/C	snv	2.0E-02	2
rs113805659	MAGI2	1.000	0.080	7	78663475	intron variant	G/C	snv	6.1E-02	2
rs12040333	ST3GAL3	1.000	0.080	1	43848369	intron variant	G/A;C	snv		2
rs1333036	CDKN2B-AS1	1.000	0.040	9	22043820	intron variant	T/C	snv	0.58	2
rs1333043	CDKN2B-AS1			9	22106732	intron variant	T/A	snv	0.64	2
rs1360589	CDKN2B-AS1	1.000	0.040	9	22045318	intron variant	C/T	snv	0.72	2
rs1360590	CDKN2B-AS1	1.000	0.040	9	22041444	intron variant	T/C;G	snv		2
rs1481805		1.000	0.080	8	71121190	intron variant	A/T	snv	0.58	2
rs1532002	LRP1B	1.000	0.080	2	140292500	intron variant	G/A	snv	2.3E-02	2
rs1537370	CDKN2B-AS1	1.000		9	22084311	intron variant	C/T	snv	0.55	2
rs1537376	CDKN2B-AS1	1.000	0.040	9	22116221	intron variant	T/C	snv	0.49	2
rs16850360				4	74006728	intron variant	A/G	snv	4.2E-02	2
rs16879003	ATXN1	1.000	0.080	6	16745008	intron variant	T/C;G	snv		2
rs16939881	ALDH1A2 ; AQP9			15	58179780	intron variant	G/C;T	snv		2
rs17214144	OSBPL3	1.000	0.080	7	24846128	intron variant	T/C	snv	0.20	2
rs2069418	CDKN2B-AS1 ; CDKN2B	1.000	0.040	9	22009699	intron variant	G/C	snv	0.70	2
rs2106119	CDKN2B-AS1	1.000	0.040	9	22017551	intron variant	A/G;T	snv		2
rs2106120	CDKN2B-AS1	1.000	0.040	9	22017102	intron variant	G/T	snv	0.56	2
rs2184061	CDKN2B-AS1	1.000	0.040	9	22061563	intron variant	C/A;T	snv	0.64	2
rs2680830	VSNL1	1.000	0.080	2	17596817	intron variant	A/G;T	snv	0.94	2
rs3798722	ELOVL2			6	11040190	intron variant	A/G	snv	0.39	2