DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Multiple Sclerosis ×

Variants associated to the Gene: CLEC16A ×

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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
rs12708716	CLEC16A	0.807	0.320	16	11086016	intron variant	A/G	snv		0.37	4
rs12927355	CLEC16A	0.882	0.240	16	11100914	intron variant	C/A;T	snv		0.29	2
rs2041670	CLEC16A	0.851	0.280	16	11080795	intron variant	G/A;C	snv			2
rs7200786	CLEC16A	0.882	0.200	16	11083944	intron variant	A/G	snv		0.59	2
rs725613	CLEC16A	0.851	0.240	16	11075826	intron variant	T/G	snv		0.42	2
rs11860603	CLEC16A	1.000	0.080	16	11071160	intron variant	T/C	snv		0.41	1
rs11865121	CLEC16A	1.000	0.080	16	11072831	intron variant	C/A	snv		0.40	1
rs2903692	CLEC16A	0.807	0.360	16	11144926	intron variant	G/A	snv		0.33	1
rs998592	CLEC16A	0.925	0.160	16	11105821	intron variant	C/T	snv		0.39	1
rs7184083	CLEC16A ; LOC105371081	1.000	0.080	16	11134057	intron variant	A/G	snv		0.72	1