DisGeNET - a database of gene-disease associations

List of shared variants

Neoplasm Metastasis, C0027627

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
rs1056123575	ADAMTS1	0.925	0.080	21	26844557	missense variant	G/A	snv	4.2E-06	7.0E-06	4
rs1131691036	TP53	0.851	0.080	17	7675207	frameshift variant	GCA/CC	delins			8
rs1172398253	CCN1	0.925	0.080	1	85582045	missense variant	C/T	snv	4.0E-06		4
rs1213469537	CAV1	0.882	0.080	7	116559145	missense variant	C/T	snv	4.0E-06	1.4E-05	9
rs1219211410	CDC25B	0.925	0.080	20	3800494	missense variant	T/C	snv			3
rs1285136498	NR3C1	0.807	0.080	5	143400101	missense variant	G/A	snv			13
rs13423759	ERBB4	0.925	0.080	2	211381247	3 prime UTR variant	A/C	snv		6.8E-02	3
rs1364963022	ESR1	0.925	0.080	6	151944233	missense variant	G/C	snv	4.0E-06		4
rs147574894	NFKB1 ; LOC105377347	0.925	0.080	4	102600911	missense variant	A/G	snv	9.6E-05	3.9E-04	4
rs16940	BRCA1	0.882	0.080	17	43093220	synonymous variant	A/G	snv	0.35	0.29	5
rs200282497	ESR1	0.925	0.080	6	151944239	missense variant	G/C	snv	3.6E-05	3.5E-05	4
rs200863613	CDKN2A	0.925	0.080	9	21971061	missense variant	C/A;T	snv	8.5E-05	3.7E-04	6
rs3731499	CDC25A	0.925	0.080	3	48184680	missense variant	G/A	snv	5.7E-05	1.2E-04	3
rs3756824	PRL ; CASC15	0.925	0.080	6	22298508	intron variant	C/G;T	snv			3
rs5780218	KISS1	0.882	0.080	1	204196482	5 prime UTR variant	A/-	delins		0.44	4
rs759478535	ERBB2	0.851	0.080	17	39708351	missense variant	A/G	snv	6.8E-05	4.2E-05	6
rs761872690	PGR ; PGR-AS1	0.925	0.080	11	101128246	synonymous variant	G/A	snv	2.8E-05		3
rs767151455	ERBB2	0.925	0.080	17	39708379	missense variant	C/T	snv	8.0E-06		4
rs773895706	RASGRF1	0.925	0.080	15	79090236	missense variant	G/A	snv	4.2E-06		3
rs776880789	PGR ; PGR-AS1	0.925	0.080	11	101128241	missense variant	G/C;T	snv	4.7E-06; 4.7E-06		4
rs79036859	DAAM1	0.925	0.080	14	59369257	3 prime UTR variant	A/G	snv			3
rs11662595	HRH4	0.882	0.120	18	24477006	missense variant	A/G	snv	8.6E-02	7.6E-02	7
rs2494752	AKT1	0.790	0.120	14	104797271	upstream gene variant	A/G	snv		0.85	10
rs4442975	LOC101928278	0.827	0.120	2	217056046	intergenic variant	G/T	snv		0.47	7
rs6464926	EZH2	0.882	0.120	7	148821919	intron variant	C/T	snv		0.41	4