DisGeNET - a database of gene-disease associations

List of associated variants

RDW - Red blood cell distribution width result, C1304746

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
rs142529006	ZKSCAN1			7	100022093	intron variant	T/A	snv		6.9E-03	4
rs603424	PKD2L1	1.000	0.080	10	100315722	intron variant	G/A	snv		0.34	13
rs7384878	STAG3L5P ; STAG3L5P-PVRIG2P-PILRB ; PMS2P1			7	100334426	intron variant	C/T	snv		0.72	2
rs72996119				11	100587081	intergenic variant	A/G	snv		7.8E-02	2
rs41295942	TFR2			7	100621008	missense variant	C/T	snv	2.0E-02	2.2E-02	2
rs717662				11	100623264	intergenic variant	C/T	snv		8.5E-02	2
rs139178017	TFR2			7	100628224	splice region variant	C/T	snv	3.1E-03	2.8E-03	2
rs9801017	TFR2			7	100638579	intron variant	G/A	snv		0.65	3
rs531909210	TFR2			7	100641799	intron variant	G/A	snv		2.8E-03	3
rs2075672	TFR2 ; ACTL6B			7	100642673	intron variant	A/G	snv		0.65	8
rs73003836	ARHGAP42			11	100713940	intron variant	C/T	snv		7.0E-02	2
rs7797559				7	101065852	intergenic variant	A/C;G;T	snv			2
rs4615960	BTRC			10	101438198	intron variant	G/A	snv		0.26	2
rs67806247	TMEM259			19	1014539	intron variant	TGATGGGGCG/-;TGATGGGGCGTGATGGGGCG	delins			2
rs636089	NCALD			8	102065562	intron variant	T/C	snv		0.28	2
rs57236717	WDR20			14	102148541	intron variant	AAA/-;A;AA;AAAA;AAAAA;AAAAAA;AAAAAAAAAA	delins			2
rs12883091	WDR20			14	102202685	intron variant	G/A	snv		0.27	2
rs3087686	MOK			14	102229226	3 prime UTR variant	A/G	snv		0.33	2
rs7692921	SLC39A8			4	102326283	intron variant	C/A	snv		0.13	2
rs368447685	NKD2			5	1025534	intron variant	T/C	snv		1.3E-03	2
rs4772494	TPP2			13	102603946	intron variant	A/G	snv		0.65	2
rs1190335	RCOR1			14	102645021	intron variant	T/C;G	snv			2
rs12764899	AS3MT ; BORCS7-ASMT	1.000	0.040	10	102875346	intron variant	G/A	snv		0.21	4
rs559546873	NT5C2			10	103186913	intron variant	AAAA/-;A;AA;AAA;AAAAA;AAAAAA	delins		0.33	2
rs17616464				14	103373661	downstream gene variant	C/G	snv		6.5E-02	2