DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: MS4A14 ×

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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
rs7935082	MS4A7 ; MS4A14	1.000	0.040	11	60387527	intron variant	T/C	snv		0.62	2
rs10501383	MS4A14	1.000	0.040	11	60397054	intron variant	C/T	snv		5.7E-02	1
rs10897056	MS4A14	1.000	0.040	11	60398982	intron variant	A/G	snv		0.71	1
rs2241920	MS4A14	1.000	0.040	11	60396731	intron variant	G/A	snv	0.65	0.62	1
rs4939352	MS4A14	1.000	0.040	11	60405634	intron variant	A/G	snv		0.67	1
rs7107802	MS4A14	1.000	0.040	11	60399149	intron variant	T/C	snv		0.69	1
rs2233244	MS4A14 ; MS4A7	1.000	0.040	11	60385058	intron variant	A/C;T	snv	0.23; 1.2E-05		1
rs3816270	MS4A14 ; MS4A7	1.000	0.040	11	60396162	5 prime UTR variant	T/C	snv		0.76	1
rs950802	MS4A7 ; MS4A14	1.000	0.040	11	60385111	synonymous variant	G/A	snv	0.35	0.36	1
rs950803	MS4A7 ; MS4A14	1.000	0.040	11	60385090	splice region variant	T/A	snv	0.64	0.60	1