DisGeNET - a database of gene-disease associations

List of shared variants

Mean blood pressure, C0428886

Disease: High density lipoprotein measurement

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
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		34
rs79105258	CUX2			12	111280427	intron variant	C/A;T	snv			24
rs12579302	ATP2B1	0.851	0.120	12	89656726	intron variant	A/G	snv		0.15	19
rs17696736	NAA25	0.827	0.240	12	112049014	intron variant	A/G	snv		0.30	18
rs7310615	SH2B3	0.882		12	111427245	intron variant	C/G	snv		0.67	12
rs4418728				10	93079967	downstream gene variant	G/T	snv		0.42	8
rs740746				10	114033028	intergenic variant	G/A	snv		0.70	8
rs2306363	SIPA1			11	65638129	5 prime UTR variant	G/T	snv		0.15	7
rs12801636	PCNX3	1.000	0.040	11	65623846	intron variant	G/A	snv		0.25	5
rs4660293	PABPC4			1	39562508	non coding transcript exon variant	A/C;G	snv			5
rs7076938	LOC105378493			10	114029616	intergenic variant	C/T	snv		0.69	3