DisGeNET - a database of gene-disease associations

Source: ALL

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
rs9890155	FAM222B			17	28798449	intron variant	A/G	snv		0.19	1
rs9891925	FAM222B			17	28777522	intron variant	A/T	snv		0.19	1
rs9898892	FAM222B			17	28823732	intron variant	T/C	snv		0.19	1
rs9905510	FAM222B			17	28765307	intron variant	G/A	snv		0.19	1
rs9906213	FAM222B			17	28770571	intron variant	A/T	snv		3.9E-03	1
rs9908881	FAM222B			17	28773906	intron variant	T/A	snv		0.19	1
rs9895443	FAM222B ; ERAL1			17	28855926	intron variant	G/A	snv		0.74	1
rs4262997	FAM222B ; RPL31P58			17	28802544	non coding transcript exon variant	A/G	snv		0.19	1