DisGeNET - a database of gene-disease associations

List of shared variants

RDW - Red blood cell distribution width result, C1304746

Disease: Monocyte count result

Source: ALL

Results per page

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
rs334	HBB	0.724	0.240	11	5227002	missense variant	T/A;C;G	snv	3.5E-03		35
rs13331259	FAM234A			16	249924	intron variant	A/G	snv		3.0E-02	14
rs112505971	ANKRD26			10	27068541	intron variant	A/C;G	snv			13
rs2853961				6	31264212	downstream gene variant	G/A	snv		0.38	13
rs3123543	ATF3			1	212617344	intron variant	T/A;C	snv			13
rs3840870	COL1A1			17	50184820	3 prime UTR variant	-/CTTG	delins			13
rs4837892	TTLL11			9	121826025	intron variant	G/T	snv		0.36	13
rs7296503	PDZRN4			12	41306962	intron variant	C/T	snv		0.57	13
rs76792961	FAM234A			16	243594	intron variant	C/T	snv		7.3E-03	13
rs7776054	HBS1L			6	135097778	intron variant	A/G	snv		0.24	13
rs9917425	OTOR			20	16755400	intron variant	G/T	snv		0.16	13
rs76428106	FLT3	0.851	0.040	13	28029870	intron variant	T/C;G	snv			10
rs35979828	NFE2			12	54292096	intron variant	C/T	snv		5.0E-02	9
rs3731211	CDKN2A			9	21986848	intron variant	T/A	snv		0.74	7
rs6475611				9	22151140	intergenic variant	G/A	snv		0.21	6
rs61745454	CCDC69			5	151187456	missense variant	A/G	snv	3.7E-02	4.6E-02	5