DisGeNET - a database of gene-disease associations

List of shared variants

Breast Carcinoma, C0678222

Disease: Non-Small Cell Lung 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
rs13312840	NBN	0.882	0.120	8	89985681	intron variant	A/G;T	snv			3
rs7211777	STAT3	0.882	0.120	17	42382057	intron variant	G/A	snv		0.52	3
rs1056503	XRCC4	0.851	0.200	5	83353158	synonymous variant	T/A;G	snv	4.0E-06; 0.23		4
rs1537514	C1orf167 ; MTHFR	0.882	0.120	1	11788011	missense variant	G/C	snv	0.10	0.10	4
rs3769821	CASP8	0.851	0.200	2	201258707	intron variant	C/T	snv		0.57	4
rs3835	XRCC5	0.882	0.120	2	216201914	intron variant	G/A	snv		0.21	4
rs755024903	NLRP2	0.851	0.200	19	54983029	missense variant	G/A;T	snv	7.5E-05; 4.2E-06		4
rs774188914	ERCC5 ; BIVM-ERCC5	0.851	0.200	13	102858296	missense variant	C/G	snv	2.4E-05	1.4E-05	4
rs781367751	LIG3	0.851	0.200	17	34991822	missense variant	A/G	snv	1.2E-05		4
rs1061302	NBN	0.827	0.160	8	89946194	synonymous variant	T/C	snv	0.35	0.30	5
rs12220909	MIR4293 ; FRMD4A	0.827	0.240	10	14383222	mature miRNA variant	G/C;T	snv	4.9E-03		5
rs1457582183	TP53	0.827	0.200	17	7673608	missense variant	G/A;C	snv		7.0E-06	5
rs28381975	PDCD6IP ; LOC105377023	0.827	0.200	3	33798239	intron variant	-/TTACGTACCTGTGCA;TTCCGTACCTGTGCA;TTTCGTACCTGTGCA	delins			5
rs50872	ERCC2	0.827	0.120	19	45359191	intron variant	A/G;T	snv			5
rs746965070	NBN	0.827	0.200	8	89955487	missense variant	T/C	snv	1.2E-05		5
rs781598341	SOD2	0.827	0.240	6	159682510	missense variant	T/C	snv	4.0E-06		5
rs1394960893	GSTP1	0.807	0.240	11	67586553	synonymous variant	C/T	snv			6
rs2227928	ATR	0.851	0.200	3	142562770	missense variant	A/G	snv	0.55	0.63	6
rs7867494	RORB	0.882	0.120	9	74529284	intron variant	A/G	snv		0.27	6
rs11662595	HRH4	0.882	0.120	18	24477006	missense variant	A/G	snv	8.6E-02	7.6E-02	7
rs3110697	IGFBP3	0.827	0.160	7	45915430	intron variant	A/G	snv		0.58	7
rs1012477	PER3	0.827	0.160	1	7798075	intron variant	G/C	snv		0.16	8
rs1061624	TNFRSF1B	0.776	0.320	1	12207208	3 prime UTR variant	A/G	snv		0.48	8
rs1799814	CYP1A1	0.807	0.160	15	74720646	missense variant	G/A;T	snv	1.6E-05; 3.1E-02		8
rs1799966	BRCA1	0.807	0.280	17	43071077	missense variant	T/A;C	snv	5.2E-05; 0.35		8