DisGeNET - a database of gene-disease associations

List of shared variants

Finding of Mean Corpuscular Hemoglobin, C1261502

Disease: Hemoglobin, CTCAE

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
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	226
rs855791	TMPRSS6	0.701	0.400	22	37066896	missense variant	A/G;T	snv	0.57; 4.0E-06		38
rs198851	H4C3			6	26104404	downstream gene variant	T/A;C;G	snv			15
rs4820268	TMPRSS6	0.851	0.160	22	37073551	missense variant	G/A;C	snv	0.53; 4.0E-06		14
rs129128	H2BC4 ; H2AC6			6	26125114	intron variant	C/T	snv		0.91	7
rs130624				22	37042611	regulatory region variant	G/T	snv		0.47	6
rs228129	LOC112268295			22	37032558	upstream gene variant	A/G	snv		0.48	6
rs2413450	TMPRSS6			22	37074184	intron variant	T/C	snv		0.61	6
rs5756520	TMPRSS6			22	37112467	upstream gene variant	G/A	snv		0.41	4