DisGeNET - a database of gene-disease associations

List of shared variants

Body Height, C0005890

Disease: Lean body mass

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
rs28778940	LOC105376157			9	95536070	intergenic variant	G/A	snv		0.31	2
rs2900208	ETV6			12	11725530	intron variant	C/A	snv		0.29	2
rs35320790	SALRNA1			14	60642107	intron variant	C/A;G	snv			2
rs3818416	EDNRB-AS1 ; EDNRB	1.000	0.080	13	77900333	intron variant	A/C	snv		0.75	2
rs4073717	FGF18			5	171437017	intron variant	G/T	snv		0.23	2
rs4373984				12	97398809	intergenic variant	C/T	snv		0.55	2
rs508347	JAZF1			7	28173205	intron variant	T/C	snv		0.69	2
rs509035	GHSR			3	172445659	intron variant	G/A	snv		0.25	2
rs55745410	PHC2			1	33337216	intron variant	A/G	snv		0.28	2
rs59985551	EFEMP1			2	55879793	intron variant	C/T	snv		0.21	2
rs62372052				5	42724192	upstream gene variant	A/G	snv		6.9E-02	2
rs6711710	KCNE4			2	223091692	intron variant	T/C	snv		0.77	2
rs6762578	COPG1			3	129273204	intron variant	G/A;T	snv			2
rs6762851	TASOR			3	56652301	intron variant	T/C	snv		0.50	2
rs6824748	LCORL			4	17995443	intron variant	G/A	snv		0.25	2
rs6899155				5	36786357	intergenic variant	T/C	snv		0.44	2
rs74494415	GALR1			18	77260182	intron variant	C/A;T	snv			2
rs76307059	SMOC2			6	168600208	intron variant	C/A;G;T	snv			2