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 EXOME	AF GENOME	Num. diseases
rs1412834	CDKN2B-AS1	0.790	0.080	9	22110132	intron variant	T/C	snv		0.64	11
rs7865618	CDKN2B-AS1	0.776	0.240	9	22031006	non coding transcript exon variant	G/A;T	snv			11
rs1333047	CDKN2B-AS1	0.790	0.240	9	22124505	intron variant	A/T	snv		0.63	9
rs10116277	CDKN2B-AS1	0.827	0.160	9	22081398	intron variant	G/T	snv		0.62	8
rs10120688	CDKN2B-AS1	0.807	0.080	9	22056500	intron variant	G/A	snv		0.50	7
rs10811656	CDKN2B-AS1	0.807	0.200	9	22124473	intron variant	C/T	snv		0.47	7
rs1333042	CDKN2B-AS1	0.827	0.120	9	22103814	intron variant	A/G	snv		0.63	7
rs523096	CDKN2B-AS1	0.827	0.080	9	22019130	intron variant	A/G	snv		0.30	7
rs7049105	CDKN2B-AS1	0.807	0.120	9	22028802	intron variant	A/G	snv		0.58	7
rs10757272	CDKN2B-AS1	0.851	0.160	9	22088261	intron variant	C/T	snv		0.41	6
rs1537375	CDKN2B-AS1	0.882	0.120	9	22116072	intron variant	T/C;G	snv			6
rs2383204	CDKN2B-AS1	0.827	0.160	9	22055049	intron variant	A/G;T	snv			6
rs496892	CDKN2B-AS1	0.827	0.160	9	22024352	intron variant	C/T	snv		0.40	6
rs634537	CDKN2B-AS1	0.851	0.080	9	22032153	intron variant	T/G	snv		0.28	6
rs9632884	CDKN2B-AS1	0.851	0.160	9	22072302	intron variant	G/A;C	snv			6
rs10738610	CDKN2B-AS1	0.882	0.120	9	22123767	intron variant	A/C;T	snv			5
rs10811650	CDKN2B-AS1	0.882	0.200	9	22067594	intron variant	A/G	snv		0.37	5
rs2891168	CDKN2B-AS1	0.851	0.160	9	22098620	intron variant	A/G	snv		0.40	5
rs3218020	CDKN2B-AS1	0.882	0.120	9	21997873	intron variant	G/A;C	snv			5
rs6475606	CDKN2B-AS1	0.882	0.080	9	22081851	intron variant	C/T	snv		0.62	5
rs944797	CDKN2B-AS1	0.882	0.120	9	22115287	intron variant	T/C;G	snv		0.49	5
rs10738607	CDKN2B-AS1	0.925	0.080	9	22088095	intron variant	A/G	snv		0.42	4
rs10757269	CDKN2B-AS1	1.000	0.040	9	22072265	intron variant	A/C;G	snv			4
rs10965215	CDKN2B-AS1	0.882	0.120	9	22029446	missense variant	G/A	snv	0.55	0.46	4
rs10965219	CDKN2B-AS1	0.882	0.080	9	22053688	intron variant	A/G	snv		0.58	4