DisGeNET - a database of gene-disease associations

List of associated variants

Body mass index procedure, C0005893

Source: GWASDB ×

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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
rs633715		1.000	0.080	1	177883445	intron variant	T/C	snv	0.17	4
rs6499640	FTO	0.925	0.160	16	53735765	intron variant	G/A	snv	0.59	4
rs731839	PEPD			19	33408159	intron variant	G/A	snv	0.63	4
rs9257809	OR12D3 ; OR5V1	0.790	0.320	6	29388554	intron variant	A/G	snv	5.8E-02	4
rs925946	BDNF-AS	0.882	0.120	11	27645655	intron variant	T/G	snv	0.72	4
rs9941349	FTO	1.000	0.080	16	53791576	intron variant	C/T	snv	0.34	4
rs10150332	NRXN3			14	79470621	intron variant	T/C	snv	0.26	3
rs10769908	STK33			11	8462542	intron variant	C/T	snv	0.55	3
rs10838738	MTCH2	1.000	0.080	11	47641497	intron variant	A/G	snv	0.28	3
rs10968576	LINGO2	0.882	0.120	9	28414341	intron variant	A/G	snv	0.26	3
rs13078807	CADM2	0.925	0.120	3	85835000	intron variant	A/G	snv	0.15	3
rs1516725	ETV5 ; DGKG	0.925	0.120	3	186106215	intron variant	T/C	snv	0.86	3
rs16986921	CTNNBL1	1.000	0.080	20	37754119	intron variant	C/T	snv	0.12	3
rs2030323	BDNF	0.925	0.080	11	27706992	intron variant	A/C	snv	0.83	3
rs2206734	CDKAL1	0.882	0.160	6	20694653	intron variant	C/T	snv	0.20	3
rs4752856	MTCH2	1.000	0.040	11	47626490	intron variant	G/A	snv	0.28	3
rs5996074	SREBF2			22	41840333	intron variant	G/A	snv	0.74	3
rs6013029	CTNNBL1	0.882	0.160	20	37771178	intron variant	G/T	snv	0.12	3
rs7647305	DGKG	1.000	0.080	3	186116501	intron variant	T/C	snv	0.74	3
rs7766070	CDKAL1	1.000	0.080	6	20686342	intron variant	C/A	snv	0.25	3
rs887912		1.000	0.080	2	59075742	intron variant	T/C;G	snv		3
rs9356744	CDKAL1	0.882	0.120	6	20685255	intron variant	T/C	snv	0.42	3
rs9368219	CDKAL1	1.000	0.080	6	20674460	intron variant	C/T	snv	0.19	3
rs9816226	DGKG	1.000	0.080	3	186116710	intron variant	A/T	snv	0.82	3
rs987237	TFAP2B	0.925	0.120	6	50835337	intron variant	A/G	snv	0.17	3