DisGeNET - a database of gene-disease associations

Source: BEFREE

Variants associated to the Disease: Malignant neoplasm of stomach ×

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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
rs2278744	HK1	0.925	0.080	10	69392716	intron variant	C/T	snv		0.18	2
rs6856901	HPSE	0.925	0.080	4	83295215	3 prime UTR variant	C/G	snv		0.27	2
rs6968084	IFRD1	0.925	0.080	7	112457066	missense variant	C/T	snv	0.17	0.16	2
rs4764887	IGF1 ; LINC02456	0.925	0.080	12	102430122	intron variant	G/A	snv		2.2E-02	2
rs3748068	IL17A	0.925	0.080	6	52190537	3 prime UTR variant	C/T	snv			2
rs9382084	IL17F	0.925	0.080	6	52240869	intron variant	G/A;T	snv			2
rs1135354	IL18R1	0.925	0.080	2	102397842	3 prime UTR variant	T/G	snv		0.23	2
rs3771157	IL18R1	0.925	0.080	2	102396972	3 prime UTR variant	C/A	snv		3.7E-02	2
rs3732131	IL1R1	0.925	0.080	2	102178143	3 prime UTR variant	A/G	snv		0.12	2
rs2472188	IL36RN	0.925	0.080	2	113063237	3 prime UTR variant	C/G	snv		0.65	2
rs2515401	IL36RN	0.882	0.080	2	113062899	3 prime UTR variant	T/A;C	snv			2
rs2515402	IL36RN	0.925	0.080	2	113063003	3 prime UTR variant	C/A	snv		0.65	2
rs3180235	IL36RN	0.882	0.080	2	113063095	3 prime UTR variant	A/G	snv		0.65	2
rs957201	IL36RN	0.925	0.080	2	113063623	3 prime UTR variant	T/C	snv		0.65	2
rs10421916	INSL3	0.925	0.080	19	17818178	intron variant	A/G	snv		0.69	2
rs2447867	ITGA1	0.925	0.080	5	52861540	missense variant	T/C;G	snv	0.79; 4.0E-06		2
rs74483926	KMT2C	0.925	0.080	7	152162598	missense variant	G/A	snv	4.8E-02	3.4E-02	2
rs11944405	LAMTOR3	0.925	0.080	4	99878804	3 prime UTR variant	T/C	snv		0.28	2
rs1230025	LOC100507053	0.925	0.080	4	99265219	intron variant	A/G;T	snv			2
rs3815254	LOC101927668	0.925	0.080	7	19943391	non coding transcript exon variant	T/C;G	snv			2
rs28361491	LOC105374440	0.925	0.080	4	44801181	intergenic variant	C/A;T	snv			2
rs34160967	LOC107984912 ; TAS1R1	0.925	0.080	1	6575246	missense variant	G/A;C	snv	0.13; 4.0E-06		2
rs579501	LOC283028	0.925	0.080	10	42751347	non coding transcript exon variant	T/G	snv		5.9E-02	2
rs73239138	MIR1269A	0.925	0.080	4	66276902	mature miRNA variant	G/A	snv	0.27	0.36	2
rs35010275	MIR196A2 ; HOXC6	0.925	0.080	12	53991008	intron variant	G/A;C	snv			2