DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: MIR99AHG ×

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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
rs9975788	MIR99AHG			21	16092495	intron variant	C/T	snv		0.32	1
rs9983980	MIR99AHG			21	16100046	intron variant	C/T	snv		0.32	1
rs11909251	MIR99AHG			21	16110067	intron variant	G/T	snv		0.33	1
rs2823615	MIR99AHG			21	16110813	intron variant	A/T	snv		0.33	1
rs2823612	MIR99AHG			21	16107233	intron variant	T/C	snv		0.32	1
rs11088565	MIR99AHG			21	16101911	intron variant	C/G;T	snv			1
rs2823819	MIR99AHG	1.000	0.040	21	16455971	intron variant	A/G	snv		0.22	1