DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: RPS9 ×

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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
rs255773	LILRB3 ; LILRA6 ; RPS9			19	54219677	intron variant	C/T	snv		0.41	1
rs4555268	LOC107985279 ; RPS9 ; LILRA6			19	54236092	intron variant	C/T	snv		0.36	1
rs112312277	RPS9			19	54202976	intron variant	G/T	snv		4.4E-02	1
rs11666543	RPS9	1.000	0.080	19	54208113	intron variant	A/G	snv		0.78	1
rs12980600	RPS9	1.000	0.080	19	54203380	intron variant	T/A	snv		0.79	1
rs35361042	RPS9			19	54244896	intron variant	C/G;T	snv			1
rs429539	RPS9			19	54248765	3 prime UTR variant	C/A;G;T	snv			1
rs73053487	RPS9			19	54245304	intron variant	T/C	snv		3.7E-02	1
rs11670934	RPS9 ; LILRA6			19	54240265	intron variant	C/G;T	snv	1.3E-02		1
rs61734497	RPS9 ; LILRA6			19	54241632	missense variant	A/C;G	snv			1