DisGeNET - a database of gene-disease associations

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Variants associated to the Gene: CHURC1-FNTB ×

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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
rs11627485	FNTB ; CHURC1-FNTB ; MAX			14	65020976	intron variant	T/C	snv		0.36	5
rs8006570	CHURC1-FNTB ; RAB15			14	64945992	3 prime UTR variant	G/A	snv		5.4E-02	4
rs7155454	FNTB ; MAX ; CHURC1-FNTB			14	65035521	intron variant	G/A	snv		0.61	4
rs7148590	CHURC1-FNTB ; FNTB ; MAX			14	65006478	intron variant	G/A	snv		0.57	3
rs11627531	CHURC1-FNTB ; FNTB ; MAX			14	65021078	intron variant	T/C	snv		0.57	2
rs8006419	FNTB ; CHURC1-FNTB ; MAX			14	65034017	intron variant	A/G	snv		0.61	2
rs726668	FNTB ; MAX ; CHURC1-FNTB			14	65029098	intron variant	A/G;T	snv			2
rs12435835	MAX ; CHURC1-FNTB ; FNTB			14	65033191	intron variant	T/G	snv		0.57	2
rs4466998	MAX ; CHURC1-FNTB ; FNTB			14	65008822	intron variant	C/A;G	snv			2
rs4899159	MAX ; FNTB ; CHURC1-FNTB			14	65013877	intron variant	A/G;T	snv			2
rs11628273	MIR4706 ; CHURC1-FNTB ; MAX ; FNTB			14	65043160	intron variant	C/T	snv		0.57	2
rs28886684	CHURC1-FNTB ; FNTB ; MAX			14	65056577	intron variant	T/C	snv		0.24	1
rs11620955	CHURC1-FNTB ; MAX ; FNTB			14	65024537	intron variant	A/G	snv		0.58	1
rs4586342	FNTB ; CHURC1-FNTB ; MAX			14	65007157	intron variant	G/A;C	snv			1
rs2296316	FNTB ; MAX ; CHURC1-FNTB			14	65053528	intron variant	T/A;C	snv			1
rs2296322	FNTB ; MAX ; CHURC1-FNTB			14	65012230	non coding transcript exon variant	T/G	snv		0.13	1
rs2412065	GPX2 ; CHURC1 ; CHURC1-FNTB			14	64940939	intron variant	C/G	snv		0.27	1
rs7158239	MAX ; CHURC1-FNTB ; FNTB			14	65053898	intron variant	G/A	snv		0.50	1
rs2898885	RAB15 ; CHURC1-FNTB			14	64954556	intron variant	T/C	snv		0.19	1