DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Finding of Mean Corpuscular Hemoglobin ×

Variants associated to the Gene: MIR4435-2HG ×

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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
rs62160676	MIR4435-2HG			2	111410354	intron variant	T/C;G	snv			5
rs143326447	MIR4435-2HG ; SOCAR	0.925	0.080	2	111511155	intron variant	T/C	snv		0.11	4
rs2009581	ACOXL ; MIR4435-2HG			2	111050100	intron variant	G/A	snv		0.26	3
rs4848370	ACOXL ; MIR4435-2HG			2	111054088	intron variant	C/T	snv		0.25	2
rs2139376	MIR4435-2HG			2	111385836	intron variant	T/C	snv		0.44	2
rs2334232	MIR4435-2HG			2	111371516	intron variant	G/A	snv		0.18	1
rs604126	MIR4435-2HG			2	111185623	intron variant	A/C;G;T	snv			1
rs616582	MIR4435-2HG			2	111184418	intron variant	T/C;G	snv			1
rs112744032	MIR4435-2HG ; SOCAR			2	111521757	intron variant	G/-	delins			1