DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Cleft Palate ×

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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
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs2910164	MIR3142HG ; MIR146A	0.447	0.880	5	160485411	mature miRNA variant	C/G	snv	0.71; 4.1E-06	0.70	193
rs79184941	FGFR2	0.617	0.600	10	121520163	missense variant	G/A;C	snv	5.6E-05; 4.0E-06		41
rs10719	DROSHA	0.677	0.680	5	31401340	3 prime UTR variant	A/G;T	snv	0.69		24
rs12229654		0.763	0.320	12	110976657	intergenic variant	T/G	snv		4.8E-03	20
rs16260	CDH1	0.716	0.440	16	68737131	upstream gene variant	C/A	snv		0.24	19
rs642961		0.732	0.440	1	209815925	intergenic variant	A/G	snv		0.84	14
rs2235371	IRF6	0.752	0.360	1	209790735	missense variant	C/T	snv	8.7E-02	3.9E-02	11
rs140291094	STAC3	0.742	0.320	12	57244322	missense variant	C/G	snv	9.1E-05	3.8E-04	11
rs522616	MMP3	0.763	0.320	11	102844317	upstream gene variant	T/C	snv		0.23	10
rs12532	MSX1	0.790	0.200	4	4863419	3 prime UTR variant	A/G	snv		0.36	10
rs587777450	PIEZO2	0.790	0.320	18	10671729	missense variant	C/T	snv			9
rs104894110	FOXE1 ; PTCSC2	0.776	0.280	9	97854108	missense variant	C/T	snv			8
rs1546124	CRISPLD2	0.807	0.200	16	84838445	5 prime UTR variant	G/A;C	snv	8.6E-06; 0.67		7
rs7650466	EPHA3	0.851	0.200	3	89481208	3 prime UTR variant	C/T	snv		0.23	7
rs2235375	IRF6	0.807	0.400	1	209792242	intron variant	G/A;C;T	snv	3.2E-05; 0.41; 4.3E-04		7
rs104893810	TGFBR2	0.790	0.360	3	30691477	missense variant	C/T	snv			7
rs4783099	CRISPLD2	0.827	0.200	16	84907723	3 prime UTR variant	C/T	snv		0.37	6
rs2486668	GRHL3	0.807	0.320	1	24331573	missense variant	C/G	snv	0.16	0.17	6
rs12229892	PTPN11	0.807	0.240	12	112485589	intron variant	G/A	snv		1.4E-02	6
rs4752028	SHTN1	0.807	0.200	10	117075480	intron variant	C/T	snv		0.73	6
rs201002930	WNT10A	0.827	0.200	2	218889997	synonymous variant	C/T	snv	3.2E-05	7.0E-06	6
rs560426	ABCA4	0.851	0.200	1	94087882	intron variant	C/T	snv		0.53	5
rs10130587	BMP4	0.851	0.200	14	53952392	intron variant	G/C	snv		0.45	5