DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Bone Density ×

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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 GENOME	Num. diseases
rs238271	LINC02341			13	42359218	intron variant	T/C	snv	0.85	1
rs238280	LINC02341			13	42364338	intron variant	T/C	snv	0.84	1
rs4811196	CTNNBL1			20	37841292	intron variant	G/A	snv	0.81	1
rs1021188				13	42541997	intergenic variant	C/T	snv	0.79	1
rs11898505	SPTBN1			2	54457420	intron variant	A/G	snv	0.76	1
rs1373004	LNCAROD ; LOC105378305			10	52668065	intron variant	T/G	snv	0.75	1
rs6752877	LOC102724072			2	54434432	regulatory region variant	G/T	snv	0.75	1
rs2504069	LOC107986529 ; ESR1			6	151764382	intron variant	C/T	snv	0.74	1
rs271170	LINC00326			6	132994665	intron variant	T/C	snv	0.74	1
rs7607093	LOC102724072			2	54432037	regulatory region variant	T/G	snv	0.74	1
rs1336981	ESR1			6	151761234	intron variant	C/T	snv	0.74	1
rs6734097				2	54424796	intergenic variant	C/T	snv	0.74	1
rs2252865	RERE	0.851	0.040	1	8362616	intron variant	T/C	snv	0.72	1
rs4342521	SEM1 ; LOC105375411			7	96506693	missense variant	T/G	snv	0.72	1
rs7781370	LOC105375411 ; SEM1			7	96504219	intron variant	T/C	snv	0.72	1
rs4427101	LOC105375412 ; SEM1			7	96512389	intron variant	T/C	snv	0.72	1
rs10085588	LOC105375412 ; SEM1 ; LOC105375411	1.000	0.080	7	96508362	intron variant	A/G	snv	0.72	1
rs1890010	LOC107986529 ; ESR1			6	151764140	intron variant	C/T	snv	0.71	1
rs712219	ESR1			6	151657304	intron variant	T/C	snv	0.70	1
rs2414095	CYP19A1 ; MIR4713HG			15	51232095	intron variant	A/G	snv	0.69	1
rs12682278	COLEC10			8	119020089	intron variant	A/G	snv	0.68	1
rs4305930	COLEC10			8	119045782	intron variant	C/T	snv	0.68	1
rs7014574	COLEC10			8	118964838	intergenic variant	C/T	snv	0.67	1
rs7006553	COLEC10			8	118958540	regulatory region variant	C/T	snv	0.67	1
rs6415470	TNFRSF11B			8	118942872	intron variant	G/A	snv	0.67	1