DisGeNET - a database of gene-disease associations

List of shared variants

Birth Weight, C0005612

Disease: Body mass index

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
rs10830963	MTNR1B	0.776	0.400	11	92975544	intron variant	C/G	snv		0.22	27
rs560887	SPC25 ; G6PC2	0.827	0.120	2	168906638	intron variant	T/C	snv	0.79	0.80	18
rs11708067	ADCY5	0.882	0.080	3	123346931	intron variant	A/G	snv		0.19	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
rs35261542	CDKAL1	1.000	0.080	6	20675561	intron variant	C/A	snv		0.26	3
rs7780752	GNGT1			7	93612328	intron variant	T/C	snv		0.27	2