DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: RFTN2 ×

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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
rs10196961	RFTN2			2	197649206	intron variant	G/A	snv		0.47	1
rs113964240	RFTN2			2	197591586	intron variant	C/A	snv		0.35	1
rs11690491	RFTN2			2	197650200	intron variant	C/T	snv		0.49	1
rs13396312	RFTN2			2	197628979	intron variant	T/A	snv		0.42	1
rs13413470	RFTN2			2	197648125	intron variant	G/A	snv		0.50	1
rs13427590	RFTN2			2	197652097	intron variant	C/T	snv		0.37	1
rs148812496	RFTN2			2	197675629	intron variant	AC/-	del		0.43	1
rs16866970	RFTN2			2	197646362	intron variant	G/A	snv		0.49	1
rs17731449	RFTN2			2	197601116	intron variant	T/C	snv		0.43	1
rs3828317	RFTN2			2	197630707	intron variant	G/C	snv		0.47	1
rs6728904	RFTN2			2	197628113	intron variant	C/T	snv		0.43	1
rs6733834	RFTN2			2	197653985	intron variant	C/G;T	snv			1
rs6748788	RFTN2			2	197668882	intron variant	G/T	snv		0.50	1
rs6757852	RFTN2			2	197665569	intron variant	G/A;T	snv			1
rs72916919	RFTN2			2	197627592	intron variant	T/G	snv		0.46	1
rs7603839	RFTN2			2	197669984	intron variant	G/A;T	snv			1
rs970552	RFTN2			2	197632788	intron variant	T/G	snv		0.49	1