J86.9

Case	Control
405	459800

Case

Control

405

459800

Top SNP Information

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds Ratio
chr3:69341874	rs116574279	FRMD4B	A>G	28	13060	24.53	7.333e-07	2.509
chr7:153351733	rs76251403	-	G>A	89	63696	21.84	2.97e-06	1.679
chr12:73869966	rs7965353	-	A>C	51	31175	21.77	3.073e-06	1.939
chr9:35917950	rs79857739	SPAAR	C>T	61	39789	20.73	5.275e-06	1.816
chr15:84116988	rs72758393	SH3GL3	C>A	63	41662	20.42	6.231e-06	1.793
chr9:118101331	rs10817752	-	T>C	301	277357	20.07	7.462e-06	1.378
chr3:134377556	rs77039092	EPHB1	G>A	30	15638	19.94	8.006e-06	2.245
chr9:119058748	rs143025231	PAPPA	T>G	24	11440	19.87	8.301e-06	2.445
chr7:96368463	rs79296503	-	C>T	94	69650	19.79	8.626e-06	1.621
chr4:176670796	rs1472324	GPM6A	T>G	241	348405	19.76	8.773e-06	0.7138
chr9:118091712	rs10817746	-	T>C	274	250282	19.41	1.056e-05	1.38
chr5:67715716	rs115252368	-	T>G	30	15882	19.29	1.12e-05	2.217
chr9:92511908	rs9330453	-	G>A	333	457751	19.12	1.227e-05	0.7356
chr11:86542769	rs77039324	PRSS23	A>G	73	51224	18.78	1.466e-05	1.69
chr4:169702511	rs13116200	PALLD	A>G	406	395005	18.71	1.523e-05	1.345
chr5:119526671	rs13164682	-	A>G	38	22088	18.62	1.592e-05	2.018
chr19:20369304	rs111453104	-	C>A	41	24499	18.62	1.597e-05	1.97
chr18:25264341	rs6508497	-	C>T	287	265965	18.57	1.636e-05	1.366
chr7:96425441	rs1879850	-	T>C	259	235062	18.55	1.652e-05	1.377
chr8:22740378	rs62495023	PEBP4	T>C	164	137533	18.49	1.707e-05	1.45

Associated Phenotypes ^ⓘ

ID	Name	Top Correlation
HP: 0001604	Vocal cord paresis	4/20
HP: 0012151	Hemothorax	1/20

Name

Top Correlation

4/20

1/20

ID	Name	Top Correlation
HP: 0000118	Phenotypic abnormality	0/20
HP: 0000707	Abnormality of the nervous system	0/20
HP: 0000924	Abnormality of the skeletal system	0/20
HP: 0000969	Edema	0/20
HP: 0001600	Abnormality of the larynx	0/20
HP: 0001605	Vocal cord paralysis	0/20
HP: 0001608	Abnormality of the voice	0/20
HP: 0001939	Abnormality of metabolism/homeostasis	0/20
HP: 0002086	Abnormality of the respiratory system	0/20
HP: 0002087	Abnormality of the upper respiratory tract	0/20
HP: 0002088	Abnormal lung morphology	0/20
HP: 0002103	Abnormality of the pleura	0/20
HP: 0002105	Hemoptysis	0/20
HP: 0002110	Bronchiectasis	0/20
HP: 0002202	Pleural effusion	0/20
HP: 0002715	Abnormality of the immune system	0/20
HP: 0002763	Abnormal cartilage morphology	0/20
HP: 0002795	Functional respiratory abnormality	0/20
HP: 0003470	Paralysis	0/20
HP: 0005607	Abnormal tracheobronchial morphology	0/20
HP: 0010978	Abnormality of immune system physiology	0/20
HP: 0011032	Abnormality of fluid regulation	0/20
HP: 0011442	Abnormal central motor function	0/20
HP: 0011842	Abnormality of skeletal morphology	0/20
HP: 0011919	Pleural empyema	0/20
HP: 0012252	Abnormal respiratory system morphology	0/20
HP: 0012337	Abnormal homeostasis	0/20
HP: 0012638	Abnormal nervous system physiology	0/20
HP: 0012647	Abnormal inflammatory response	0/20
HP: 0012649	Increased inflammatory response	0/20
HP: 0012735	Cough	0/20
HP: 0025044	Lung abscess	0/20
HP: 0025142	Constitutional symptom	0/20
HP: 0025424	Abnormal larynx physiology	0/20
HP: 0025426	Abnormal bronchus morphology	0/20
HP: 0025615	Abscess	0/20
HP: 0030166	Night sweats	0/20
HP: 0031245	Productive cough	0/20
HP: 0031801	Vocal cord dysfunction	0/20
HP: 0032016	Abnormal sputum	0/20
HP: 0032251	Abnormal immune system morphology	0/20
HP: 0100662	Chondritis	0/20

Name

Top Correlation

HP: 0000118

Phenotypic abnormality

0/20

HP: 0000707

Abnormality of the nervous system

0/20

HP: 0000924

Abnormality of the skeletal system

0/20

HP: 0000969