DisGeNET - a database of gene-disease associations

List of shared variants

Red cell distribution width determination, C0427460

Disease: Cardiovascular Diseases

Source: INFERRED ×

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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
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	38
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	36
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	22
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		14
rs28601761		1.000	0.040	8	125487789	intron variant	C/G	snv		0.37	13
rs603424	PKD2L1	1.000	0.080	10	100315722	intron variant	G/A	snv		0.34	13
rs415895	SWAP70			11	9748015	missense variant	C/G	snv	0.62	0.61	6