DisGeNET - a database of gene-disease associations

List of associated variants

Malignant neoplasm of pancreas, C0346647

Source: ALL

Results per page

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
rs1339638227	CDKN2A	0.925	0.120	9	21971119	missense variant	T/C	snv	4.3E-06		2
rs6475609	CDKN2B-AS1	0.925	0.120	9	22106272	intron variant	A/C;G;T	snv			2
rs488087	CEL	0.925	0.120	9	133071212	synonymous variant	C/A;T	snv	0.11	0.26	2
rs2236479	COL18A1 ; SLC19A1	0.925	0.160	21	45499218	intron variant	G/A	snv		0.40	2
rs747601652	CRYZ	0.925	0.120	1	74723233	missense variant	A/G	snv	1.2E-05		2
rs1810205	CUBN	0.925	0.120	10	16923228	intron variant	A/G	snv		0.47	2
rs6127119	CYP24A1	0.925	0.120	20	54162543	intron variant	C/T	snv		0.24	2
rs6464375	DPP6	0.925	0.120	7	153928758	intron variant	C/T	snv		6.7E-02	2
rs876661110	FBXO11 ; MSH6	0.925	0.120	2	47791093	missense variant	G/A	snv			2
rs7993418	FLT1	0.925	0.120	13	28308924	synonymous variant	G/A	snv	0.80	0.67	2
rs371609024	FUT8	0.925	0.120	14	65629530	missense variant	A/G	snv	4.0E-06		2
rs199474357	HLA-A	0.925	0.120	6	29942790	missense variant	T/C;G	snv			2
rs4795218	HNF1B ; LOC105371754	0.925	0.120	17	37718512	intron variant	A/G	snv		0.82	2
rs200349340	HOTAIR	0.925	0.120	12	53962704	non coding transcript exon variant	T/A;G	snv			2
rs201753355	HTATSF1P2 ; NQO2	0.925	0.120	6	3019647	missense variant	G/A;C	snv	2.0E-05		2
rs13303010	KLHL17 ; NOC2L	0.925	0.120	1	959193	intron variant	G/A	snv	0.82	0.69	2
rs12456874	LDLRAD4	0.925	0.120	18	13366863	intron variant	A/G	snv		0.20	2
rs1455311	LINC01088	0.925	0.160	4	79043433	intron variant	A/G	snv		0.14	2
rs1318	LOC101928045 ; PITPNC1	0.925	0.120	17	67695266	3 prime UTR variant	A/G	snv		0.30	2
rs1810636	LOC105372507	0.925	0.160	20	2674279	regulatory region variant	A/C;T	snv			2
rs1547374	LOC105372815	0.925	0.120	21	42358786	downstream gene variant	A/G	snv		0.32	2
rs782095550	MANF	0.925	0.120	3	51386267	missense variant	T/C	snv			2
rs12939944	MAP2K4	0.925	0.120	17	12056502	intron variant	C/T	snv		0.45	2
rs141095230	MGMT	0.925	0.120	10	129536277	missense variant	C/A;T	snv	8.0E-06; 5.2E-05		2
rs3021088	ND2 ; COX1	0.925	0.120	MT	5460	missense variant	G/A	snv			2