DisGeNET - a database of gene-disease associations

Source: GWASCAT

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 GENOME	Num. diseases
rs3862469	CLEC16A	1.000	0.040	16	11100223	intron variant	C/T	snv	0.35	1
rs17806299	CLEC16A	1.000	0.080	16	11106123	intron variant	G/A	snv	0.15	1
rs9923856	CLEC16A	1.000	0.080	16	11116558	intron variant	T/C	snv	0.41	1
rs12708715	CLEC16A	1.000	0.080	16	11083967	intron variant	C/T	snv	0.39	1
rs725613	CLEC16A	0.851	0.240	16	11075826	intron variant	T/G	snv	0.42	1
rs2903692	CLEC16A	0.807	0.360	16	11144926	intron variant	G/A	snv	0.33	1
rs12708716	CLEC16A	0.807	0.320	16	11086016	intron variant	A/G	snv	0.37	1
rs887864	CLEC16A	0.925	0.120	16	11065028	intron variant	G/A;C;T	snv		1
rs248831	CLEC16A			16	11187361	intergenic variant	G/A	snv	0.31	1
rs2041670	CLEC16A	0.851	0.280	16	11080795	intron variant	G/A;C	snv		1
rs9652601	CLEC16A	1.000	0.080	16	11080508	intron variant	G/A	snv	0.34	1
rs12599402	CLEC16A	0.925	0.160	16	11096031	intron variant	T/C	snv	0.51	1
rs8054198	CLEC16A	1.000	0.080	16	10944503	upstream gene variant	C/T	snv	6.7E-02	1
rs11865121	CLEC16A	1.000	0.080	16	11072831	intron variant	C/A	snv	0.40	1
rs6498160	CLEC16A	1.000	0.080	16	11105590	intron variant	T/C	snv	0.51	1
rs6498168	CLEC16A	1.000	0.080	16	11141273	intron variant	T/G	snv	0.71	1
rs17229044	CLEC16A	1.000	0.120	16	10969079	intron variant	C/T	snv	0.16	1
rs8061043	CLEC16A			16	11067072	intron variant	G/T	snv	0.19	1
rs6498142	CLEC16A			16	10987392	intron variant	C/G	snv	0.77	1
rs876476	CLEC16A			16	11056391	intron variant	G/A	snv	0.26	1
rs12924112	CLEC16A	1.000	0.120	16	11125863	intron variant	T/A;G	snv		1
rs2041733	CLEC16A ; LOC105371081	1.000	0.120	16	11135732	intron variant	T/C;G	snv		1
rs62026377	LOC105371081 ; CLEC16A			16	11135271	intron variant	G/T	snv	0.23	1
rs12935657	CLEC16A	0.925	0.080	16	11125184	intron variant	G/A	snv	0.18	2
rs12924729	CLEC16A	0.882	0.200	16	11093926	intron variant	G/A	snv	0.34	2