DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: FAM222B ×

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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
rs9892942	FAM222B			17	28851743	intron variant	C/T	snv		0.25	3
rs12946844	FAM222B			17	28843138	intron variant	C/G;T	snv			2
rs35033748	FAM222B			17	28852572	intron variant	T/C	snv		0.26	2
rs9914988	ERAL1 ; FAM222B			17	28856086	intron variant	G/A	snv		0.74	1
rs28847895	FAM222B			17	28845502	intron variant	T/C;G	snv		0.26	1
rs7215310	FAM222B			17	28761608	intron variant	C/A	snv		0.19	1
rs11650788	FAM222B			17	28847505	intron variant	T/A	snv		0.25	1
rs57583458	FAM222B			17	28779752	intron variant	TAAATAAATAAATAAATAAATAAATAAA/-;TAAATAAATAAA;TAAATAAATAAATAAA;TAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAATAAATAAATAAA	delins			1