DisGeNET - a database of gene-disease associations

List of shared variants

Autistic Disorder, C0004352

Disease: Autism Spectrum Disorders

Source: ALL

Results per page

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
rs3746544	SNAP25 ; SNAP25-AS1	0.790	0.120	20	10306436	3 prime UTR variant	G/T	snv		0.68	10
rs1051312	SNAP25 ; SNAP25-AS1	0.827	0.120	20	10306440	3 prime UTR variant	T/C	snv		0.20	5
rs35678	ATP2B2	0.925	0.040	3	10338239	missense variant	C/T	snv	0.49	0.47	2
rs736707	LOC101927870 ; RELN	0.851	0.040	7	103489956	intron variant	A/G	snv		0.30	6
rs2278556	ATP2B2	0.925	0.040	3	10360419	intron variant	G/A	snv		0.34	2
rs362691	RELN	0.882	0.120	7	103610714	missense variant	G/A;C;T	snv	1.2E-05; 0.12		3
rs10498676	ELOVL2	0.925	0.040	6	11026766	intron variant	G/A	snv		0.18	3
rs25925	CAMK4	0.925	0.040	5	111484055	synonymous variant	G/C	snv	0.75	0.83	2
rs167771	DRD3	0.827	0.280	3	114157428	intron variant	G/A;T	snv			5
rs1858830	MET	0.925	0.040	7	116672385	5 prime UTR variant	C/G	snv		0.40	4
rs2896218	WNT2	0.925	0.040	7	117279924	intron variant	G/A	snv		0.60	2
rs6950765	WNT2	0.925	0.040	7	117281176	intron variant	C/G	snv		0.64	2
rs397507444	MTHFR	0.405	0.880	1	11794407	missense variant	T/G	snv			306
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs201551401	GPR37	0.925	0.040	7	124746694	missense variant	C/T	snv	6.4E-05	1.4E-05	3
rs1881084	SND1	0.925	0.040	7	127704626	intron variant	G/A	snv		0.33	2
rs370911031	NCS1	0.925	0.040	9	130219801	missense variant	G/A	snv	1.5E-04	8.4E-05	2
rs28364997	SLC6A3	0.807	0.120	5	1403013	missense variant	G/A	snv	5.3E-04	5.8E-04	9
rs756472	MRTFB	0.925	0.040	16	14185624	intron variant	G/A	snv		0.24	2
rs7794745	CNTNAP2	0.851	0.040	7	146792514	intron variant	A/T	snv		0.49	6
rs4141463	MACROD2	0.925	0.040	20	14766825	intron variant	T/C	snv		0.50	3
rs2710102	CNTNAP2	0.790	0.120	7	147877298	intron variant	A/G;T	snv			12
rs1799971	OPRM1	0.559	0.600	6	154039662	missense variant	A/G	snv	0.19	0.12	95
rs6150410		0.925	0.040	7	155454910	intron variant	CGCATCCCC/-;CGCATCCCCCGCATCCCC	delins		0.28	2
rs34808376		0.925	0.040	7	155456016	intron variant	-/GC	delins			2