DisGeNET - a database of gene-disease associations

List of shared variants

Bronchopulmonary Dysplasia, C0006287

Disease: Borderline Personality Disorder

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
rs10994336	ANK3	0.776	0.160	10	60420054	intron variant	C/T	snv		7.5E-02	12
rs11199993	FGFR2	0.925	0.120	10	121531750	intron variant	G/C	snv		4.8E-02	2
rs1128306	HCG9 ; HLA-A	0.925	0.120	6	29975492	non coding transcript exon variant	G/A	snv		0.22	2
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs12290811	TENM4	0.882	0.120	11	79372576	intron variant	T/A	snv		0.18	3
rs1311223100	SLC18A1	0.925	0.120	8	20180955	frameshift variant	T/-	del	5.2E-06		2
rs1344706	ZNF804A	0.701	0.160	2	184913701	intron variant	A/C;T	snv			21
rs1386494	TPH2	0.790	0.120	12	71958763	intron variant	T/C;G	snv		0.82	7
rs1390938	SLC18A1	0.807	0.200	8	20179202	missense variant	A/G	snv	0.71	0.78	7
rs1497020	SLC18A1	0.925	0.120	8	20144915	3 prime UTR variant	G/A	snv		0.75	2
rs1610037	ADCYAP1	0.925	0.120	18	910634	3 prime UTR variant	A/G	snv		0.26	2
rs165599	ARVCF ; COMT	0.677	0.280	22	19969258	3 prime UTR variant	G/A	snv		0.56	27
rs1705236	TSPAN8	0.827	0.200	12	71151778	intron variant	T/A	snv		7.6E-02	5
rs174576	FADS2	0.851	0.200	11	61836038	intron variant	C/A;T	snv			14
rs175174	ZDHHC8	0.882	0.120	22	20140031	non coding transcript exon variant	A/G	snv		0.44	3
rs187269	GABRB2	0.827	0.160	5	161329618	3 prime UTR variant	A/G	snv		0.34	6
rs1938516	ERVMER61-1	0.925	0.120	1	187433789	intron variant	T/A	snv		5.7E-02	2
rs2066713	SLC6A4	0.807	0.200	17	30224647	intron variant	G/A	snv		0.34	9
rs2070744	NOS3	0.608	0.680	7	150992991	intron variant	C/T	snv		0.70	54
rs2230912	P2RX7 ; LOC105370032	0.752	0.280	12	121184393	missense variant	A/G	snv	0.13	0.12	16
rs2251219	SMIM4 ; PBRM1	0.732	0.120	3	52550771	synonymous variant	T/C;G	snv	0.39; 4.0E-06	0.34	14
rs2270637	SLC18A1	0.882	0.120	8	20179316	missense variant	C/G	snv	0.20	0.21	3
rs2270641	SLC18A1	0.882	0.120	8	20180955	missense variant	T/C;G	snv	0.32		3
rs2279709	SLC18A1	0.882	0.120	8	20178722	intron variant	T/G	snv		0.51	5
rs2284017	CACNG2	0.925	0.120	22	36700882	intron variant	T/C	snv		0.44	2