DisGeNET - a database of gene-disease associations

List of shared variants

Diabetes Mellitus, C0011849

Disease: Breast Carcinoma

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
rs2241745	IRS2	0.882	0.120	13	109770184	intron variant	C/T	snv		0.88	4
rs2605039	HSPD1	0.882	0.120	2	197498127	intron variant	C/A	snv		0.71	4
rs4876369	SLC30A8 ; LOC105375716	0.882	0.120	8	117151265	intron variant	A/G	snv		0.10	4
rs11915160	SOX2 ; SOX2-OT	0.851	0.200	3	181713783	3 prime UTR variant	C/A	snv		0.11	5
rs2188380	LINC01405	0.851	0.200	12	110948323	intron variant	T/C	snv		4.7E-03	6
rs10636	MT2A	0.851	0.160	16	56609431	3 prime UTR variant	G/C	snv		0.26	7
rs11212617	C11orf65	0.827	0.200	11	108412434	intron variant	C/A	snv		0.49	7
rs12325817	PEMT	0.807	0.320	17	17583205	intron variant	C/A;G;T	snv			7
rs1520220	LINC02456 ; IGF1	0.807	0.280	12	102402744	intron variant	G/C;T	snv		0.76	9
rs1862513	RETN	0.763	0.360	19	7668907	upstream gene variant	C/G;T	snv			11
rs1693482	ADH1C ; ADH1B	0.807	0.240	4	99342808	missense variant	C/T	snv	0.34	0.31	12
rs2230774	ROCK2	0.807	0.240	2	11218994	missense variant	G/C;T	snv	0.49		12
rs228648	UTS2	0.776	0.360	1	7853370	missense variant	G/A	snv	0.51	0.52	13
rs2072668	OGG1	0.732	0.280	3	9756456	intron variant	C/G	snv	0.28	0.24	14
rs184003	AGER	0.724	0.400	6	32182519	intron variant	C/A	snv	0.12	0.12	15
rs2890565	UTS2	0.732	0.440	1	7849677	missense variant	C/T	snv	8.7E-02	5.6E-02	15
rs4149117	SLCO1B3-SLCO1B7 ; SLCO1B3	0.763	0.360	12	20858546	missense variant	T/C;G	snv	0.81		15
rs11196172	TCF7L2	0.708	0.200	10	112967084	intron variant	G/A	snv		0.13	18
rs5744168	TLR5	0.701	0.480	1	223111858	stop gained	G/A	snv	5.3E-02	4.4E-02	18
rs2073618	COLEC10 ; TNFRSF11B	0.716	0.480	8	118951813	missense variant	G/C	snv	0.52	0.60	19
rs16917496	KMT5A	0.689	0.360	12	123409283	3 prime UTR variant	C/G;T	snv			21
rs4402960	IGF2BP2	0.724	0.400	3	185793899	intron variant	G/T	snv		0.38	21
rs4746	GLO1	0.708	0.400	6	38682852	missense variant	T/A;G	snv	0.36		21
rs10811661		0.724	0.400	9	22134095	intergenic variant	T/C	snv		0.14	22
rs1805097	IRS2	0.689	0.360	13	109782884	missense variant	C/G;T	snv	0.35		22