DisGeNET - a database of gene-disease associations

List of shared variants

Blood basophil count (lab test), C0200641

Disease: Eosinophil count procedure

Source: GWASCAT ×

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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
rs3810328	SYMPK ; FOXA3			19	45864964	intron variant	G/T	snv		1.0E-01	2
rs705699	SUOX ; RAB5B	0.882	0.160	12	55991020	non coding transcript exon variant	G/A	snv		0.40	5
rs113422568	SUFU			10	102578181	intron variant	G/A	snv		0.25	2
rs2038700	STXBP6			14	24992783	intron variant	T/C	snv		0.53	7
rs7141943	STXBP6			14	24969044	intron variant	A/G;T	snv			3
rs2115536	ST20-MTHFS ; ST20			15	79901905	intron variant	C/T	snv		0.50	2
rs2072735	SPSB1			1	9295413	intron variant	A/C	snv		0.76	2
rs7569084	SPRED2			2	65429835	intron variant	C/T	snv		0.62	2
rs139707092	SPC25 ; NOSTRIN			2	168850753	intron variant	TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT	delins			5
rs796650675	SP140			2	230312486	intron variant	TT/-;T;TTT	delins			2
rs2033784	SMAD3	1.000	0.080	15	67157322	intron variant	A/G	snv		0.35	3
rs663045	SLC25A24			1	108200437	5 prime UTR variant	G/C	snv		0.55	5
rs35188965	SLC12A7			5	1104823	intron variant	C/G;T	snv			12
rs77204473	SIK3			11	116934348	intron variant	T/C;G	snv			2
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		61
rs12968338	SERPINB13			18	63584740	upstream gene variant	C/G;T	snv			2
rs61731111	S1PR4			19	3179519	missense variant	C/G;T	snv	1.3E-02		2
rs10409243	S1PR2 ; DNMT1			19	10222312	3 prime UTR variant	C/A;G;T	snv			6
rs28567906	RUNX1			21	34911514	intron variant	A/G	snv		0.16	2
rs56117721	RUNX1			21	35026289	intron variant	T/A	snv		5.3E-02	2
rs8133974	RUNX1			21	35078544	intron variant	C/T	snv		0.11	3
rs9979383	RUNX1	0.925	0.200	21	35343463	intron variant	C/G;T	snv			5
rs13315649	RPN1			3	128672379	intron variant	T/A	snv		0.24	2
rs11624512	RIN3			14	92644775	non coding transcript exon variant	C/T	snv		0.15	5
rs140948517	RHBDD2			7	75857462	intron variant	TT/-;T;TTT;TTTT;TTTTTTTTTTTT	delins			2