DisGeNET - a database of gene-disease associations

List of shared variants

Systolic Pressure, C0871470

Disease: Birth Weight

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
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			93
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		92
rs1801253	ADRB1	0.683	0.440	10	114045297	missense variant	G/C	snv	0.74	0.69	34
rs3918226	NOS3	0.925	0.080	7	150993088	intron variant	C/T	snv		5.7E-02	12
rs17367504	MTHFR	1.000	0.040	1	11802721	intron variant	A/G	snv		0.14	9
rs72681869	SOS2			14	50188639	missense variant	G/A;C	snv	4.0E-06; 4.1E-03		6
rs76895963	CCND2-AS1 ; CCND2	1.000	0.080	12	4275678	intron variant	T/G	snv		1.5E-02	6
rs2282978	LOC112268009 ; CDK6			7	92635096	intron variant	T/C	snv		0.38	5
rs2229742	NRIP1			21	14966851	missense variant	G/C	snv	7.9E-02	7.1E-02	3
rs12909648	AKAP13			15	85681339	intron variant	G/A	snv		0.40	2
rs2428362				17	7276955	upstream gene variant	C/A;T	snv			2