DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: CSMD1 ×

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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
rs673465	LOC105377792 ; CSMD1	1.000	0.040	8	3000838	intron variant	C/G	snv	0.87	1
rs2406305	CSMD1	1.000	0.040	8	3160861	intron variant	C/T	snv	0.85	1
rs2688325	CSMD1			8	3909688	intron variant	T/C	snv	0.63	1
rs2627395	CSMD1			8	3921330	intron variant	C/T	snv	0.58	1
rs10503256	CSMD1	1.000	0.040	8	4356657	intron variant	A/G	snv	0.57	1
rs12550650	CSMD1			8	4693468	intron variant	C/T	snv	0.49	1
rs7828501	CSMD1			8	4702559	intron variant	A/G	snv	0.48	1
rs17079504	CSMD1	1.000	0.040	8	3161800	intron variant	G/A	snv	0.30	1
rs4266671	CSMD1			8	4971671	intron variant	A/G	snv	0.27	1
rs67121641	CSMD1			8	4936142	intron variant	C/G	snv	0.26	1
rs7463166	CSMD1			8	4976268	intron variant	A/G	snv	0.26	1
rs13261217	CSMD1	1.000	0.040	8	4325535	non coding transcript exon variant	A/G	snv	0.26	1
rs13260434	CSMD1	0.925	0.040	8	3368702	intron variant	T/A	snv	0.24	2
rs11998250	CSMD1	1.000	0.040	8	3162070	intron variant	A/C	snv	0.22	1
rs592700	LOC105377792 ; CSMD1	1.000	0.040	8	3008823	intron variant	T/C	snv	0.21	1
rs10503253	CSMD1	0.851	0.040	8	4323322	intron variant	C/A	snv	0.18	5
rs13277378	LOC105377792 ; CSMD1	1.000	0.040	8	3008416	intron variant	C/T	snv	0.18	1
rs9987128	CSMD1	1.000	0.040	8	3122601	intron variant	A/G	snv	0.17	1
rs11987640	CSMD1	1.000		8	4584258	intron variant	G/C	snv	0.12	2
rs11136775	CSMD1	0.925	0.040	8	4791194	intron variant	G/C	snv	0.12	2
rs17079498	CSMD1	1.000	0.040	8	3160822	intron variant	T/C	snv	7.1E-02	1
rs4876060	LOC105377792 ; CSMD1	1.000	0.040	8	3013377	intron variant	A/T	snv	7.0E-02	1
rs17079506	CSMD1	1.000	0.040	8	3162901	intron variant	T/A	snv	6.8E-02	1
rs73660619	CSMD1	1.000	0.080	8	3230651	intron variant	T/C	snv	6.8E-02	1
rs1460403	CSMD1	1.000	0.040	8	3162709	intron variant	T/A	snv	5.0E-02	1