DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: OASL ×

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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
rs3213545	OASL			12	121033534	synonymous variant	G/A	snv	0.32	0.26	3
rs7957197	OASL	0.925	0.120	12	121022883	intron variant	T/A	snv		0.18	2
rs10774580	OASL			12	121038620	intron variant	A/G	snv		0.55	1
rs2259883	OASL			12	121024336	intron variant	G/A;C	snv			1
rs2708081	OASL			12	121025485	intron variant	T/C	snv		0.51	1
rs61953351	OASL	1.000	0.080	12	121018813	upstream gene variant	G/T	snv		0.25	1