DisGeNET - a database of gene-disease associations

List of associated variants

Meningioma, benign, no ICD-O subtype, C1762616

Source: ALL

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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
rs9420907	STN1	0.790	0.320	10	103916707	intron variant	C/A;G	snv			7
rs2736100	TERT	0.550	0.880	5	1286401	3 prime UTR variant	C/A	snv		0.52	83
rs768803947	TP53	0.882	0.080	17	7670624	missense variant	C/A;T	snv	4.0E-06; 4.0E-06		3
rs730882035	VHL	0.807	0.200	3	10149805	missense variant	G/A	snv			7
rs7574920	XDH	0.882	0.080	2	31362783	intron variant	G/C	snv		0.42	3