DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: H2BC4 ×

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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
rs129128	H2BC4 ; H2AC6			6	26125114	intron variant	C/T	snv		0.91	7
rs707896	H2BC4			6	26116196	intron variant	G/A	snv		0.18	3
rs198825	H2AC6 ; H2BC4	0.925	0.120	6	26122274	intron variant	A/G	snv		0.46	2
rs198820	H2AC6 ; H2BC4	0.925	0.120	6	26124015	upstream gene variant	G/A	snv		0.29	2
rs198821	H2AC6 ; H2BC4	0.925	0.120	6	26123401	3 prime UTR variant	T/C	snv		0.48	2
rs198823	H2AC6 ; H2BC4			6	26122705	intron variant	G/C;T	snv			2
rs198828	H2BC4	0.925	0.120	6	26119231	intron variant	G/A	snv		0.46	2
rs198827	H2BC4	0.925	0.120	6	26120774	intron variant	C/T	snv		0.48	2
rs198826	H2BC4	0.925	0.120	6	26120925	intron variant	C/G;T	snv			2
rs12206204	H2BC4			6	26116754	intron variant	C/T	snv		1.1E-02	2
rs1773284	H2AC6 ; H2BC4			6	26122225	intron variant	C/A	snv		0.17	1
rs16891325	H2BC4			6	26118439	intron variant	T/C	snv		0.12	1