J36

Case	Control
514	459680

Case

Control

514

459680

Top SNP Information

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds Ratio
chr1:58800895	rs77919581	DAB1	C>A	42	16571	28.21	1.088e-07	2.259
chr7:32405947	rs182494	PDE1C	A>C	56	25896	25.79	3.811e-07	1.982
chr19:1546944	rs10406647	-	A>G	295	200821	25.07	5.541e-07	1.404
chr7:21814839	rs17145367	DNAH11	A>G	94	50787	24.77	6.464e-07	1.701
chr7:32415383	rs399902	PDE1C	A>G	54	25314	23.06	1.572e-06	1.932
chr3:177740326	rs62283984	-	A>G	47	21098	22.87	1.737e-06	2.012
chr6:153923555	rs76329855	-	C>T	143	86411	22.64	1.953e-06	1.528
chr7:32414516	rs215714	PDE1C	G>A	56	26868	22.34	2.282e-06	1.893
chr2:216287234	rs79603802	FN1	C>T	33	13259	22.03	2.681e-06	2.245
chr13:62869973	rs1328334	-	T>G	59	28787	21.96	2.781e-06	1.855
chr9:28921331	rs117994625	-	C>T	48	22020	21.91	2.863e-06	1.971
chr22:29236402	rs76205571	-	T>C	63	31614	21.53	3.478e-06	1.811
chr3:55854551	rs76934414	ERC2	A>G	44	19770	21.36	3.81e-06	2.009
chr7:32411504	rs215712	PDE1C	C>A	51	24201	21.34	3.847e-06	1.919
chr7:21830243	rs28611316	DNAH11	T>C	115	67895	20.92	4.793e-06	1.564
chr15:94768663	rs16948815	-	G>A	31	12410	20.86	4.948e-06	2.25
chr19:6922735	rs252564	ADGRE1	C>T	341	244319	20.64	5.536e-06	1.344
chr3:177664238	rs62283964	-	C>T	43	19531	20.24	6.843e-06	1.988
chr12:59160942	rs1353611	-	G>A	137	84023	20.13	7.242e-06	1.502
chr7:32446402	rs76212094	PDE1C	G>A	29	11460	20.07	7.473e-06	2.272

Associated Phenotypes ^ⓘ

ID	Name	Top Correlation
HP: 0000211	Trismus	1/20

Name

Top Correlation

HP: 0000211

Trismus

1/20

ID	Name	Top Correlation
HP: 0000118	Phenotypic abnormality	0/20
HP: 0000152	Abnormality of head or neck	0/20
HP: 0000153	Abnormality of the mouth	0/20
HP: 0000234	Abnormality of the head	0/20
HP: 0000271	Abnormality of the face	0/20
HP: 0000277	Abnormality of the mandible	0/20
HP: 0000366	Abnormality of the nose	0/20
HP: 0000600	Abnormality of the pharynx	0/20
HP: 0000924	Abnormality of the skeletal system	0/20
HP: 0000929	Abnormal skull morphology	0/20
HP: 0001626	Abnormality of the cardiovascular system	0/20
HP: 0001739	Abnormality of the nasopharynx	0/20
HP: 0002086	Abnormality of the respiratory system	0/20
HP: 0002088	Abnormal lung morphology	0/20
HP: 0002205	Recurrent respiratory infections	0/20
HP: 0002597	Abnormality of the vasculature	0/20
HP: 0002715	Abnormality of the immune system	0/20
HP: 0002719	Recurrent infections	0/20
HP: 0002788	Recurrent upper respiratory tract infections	0/20
HP: 0009121	Abnormal axial skeleton morphology	0/20
HP: 0010978	Abnormality of immune system physiology	0/20
HP: 0011110	Tonsillitis	0/20
HP: 0011821	Abnormality of facial skeleton	0/20
HP: 0011842	Abnormality of skeletal morphology	0/20
HP: 0011947	Respiratory tract infection	0/20
HP: 0012252	Abnormal respiratory system morphology	0/20
HP: 0025031	Abnormality of the digestive system	0/20
HP: 0025033	Abnormality of digestive system morphology	0/20
HP: 0025439	Pharyngitis	0/20
HP: 0025615	Abscess	0/20
HP: 0030791	Abnormal jaw morphology	0/20
HP: 0030812	Enlarged tonsils	0/20
HP: 0032101	Unusual infection	0/20
HP: 0032251	Abnormal immune system morphology	0/20
HP: 0100763	Abnormality of the lymphatic system	0/20
HP: 0100765	Abnormality of the tonsils	0/20
HP: 0100776	Recurrent pharyngitis	0/20

Name

Top Correlation

HP: 0000118

Phenotypic abnormality

0/20

HP: 0000152

Abnormality of head or neck

0/20

HP: 0000153

Abnormality of the mouth

0/20

HP: 0000234