O12.0

Case	Control
88	460118

Case

Control

460118

Top SNP Information

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds Ratio
chr6:15766186	rs407994	-	A>G	12	12215	36.93	1.222e-09	5.083
chr4:72885186	rs115201553	-	A>G	12	13150	33.53	7.002e-09	4.77
chr7:17632452	rs73080733	-	A>C	11	11538	32.33	1.303e-08	4.911
chr14:47667128	rs61995417	MDGA2	A>C	22	35857	30.56	3.234e-08	3.257
chr10:121166534	rs118162653	GRK5	C>A	11	12150	29.83	4.727e-08	4.659
chr3:183342891	rs73190859	-	G>A	15	20375	29.14	6.72e-08	3.844
chr3:184498664	rs76934365	-	A>C	27	50794	28.48	9.467e-08	2.874
chr7:4149918	rs6965018	SDK1	C>T	14	19991	26.75	2.31e-07	3.803
chr15:74244902	rs117868043	-	G>A	12	15254	26.45	2.708e-07	4.106
chr8:3503814	rs57884893	CSMD1	T>C	12	15071	26.44	2.721e-07	4.103
chr7:73476096	rs77275979	ELN	A>C	13	17071	26.39	2.794e-07	3.919
chr4:29403914	rs17717410	-	A>G	29	59086	25.61	4.187e-07	2.659
chr3:9554359	rs11710200	LHFPL4	T>C	23	42430	24.86	6.159e-07	2.876
chr5:151096944	rs982688	-	T>C	111	398895	24.31	8.188e-07	2.046
chr17:74623865	rs78856096	ST6GALNAC1	G>C	13	19175	23.6	1.187e-06	3.687
chr21:26124303	rs76095499	-	A>G	12	16287	23.52	1.237e-06	3.83
chr19:38534650	rs73040879	SIPA1L3	G>A	9	10357	23.22	1.443e-06	4.484
chr2:125092113	rs11694014	CNTNAP5	C>A	27	55819	22.92	1.69e-06	2.598
chr21:33552512	rs2833693	-	T>C	86	280701	22.75	1.843e-06	1.967
chr3:35483706	rs73066679	-	T>C	10	12434	22.37	2.25e-06	4.115

Associated Phenotypes ^ⓘ

ID	Name	Top Correlation
HP: 0002789	Tachypnea	2/20

Name

Top Correlation

HP: 0002789

Tachypnea

2/20

ID	Name	Top Correlation
HP: 0000079	Abnormality of the urinary system	0/20
HP: 0000093	Proteinuria	0/20
HP: 0000118	Phenotypic abnormality	0/20
HP: 0000119	Abnormality of the genitourinary system	0/20
HP: 0000924	Abnormality of the skeletal system	0/20
HP: 0001385	Hip dysplasia	0/20
HP: 0001871	Abnormality of blood and blood-forming tissues	0/20
HP: 0001881	Abnormal leukocyte morphology	0/20
HP: 0001909	Leukemia	0/20
HP: 0001928	Abnormality of coagulation	0/20
HP: 0001939	Abnormality of metabolism/homeostasis	0/20
HP: 0001977	Abnormal thrombosis	0/20
HP: 0002086	Abnormality of the respiratory system	0/20
HP: 0002644	Abnormality of pelvic girdle bone morphology	0/20
HP: 0002664	Neoplasm	0/20
HP: 0002715	Abnormality of the immune system	0/20
HP: 0002793	Abnormal pattern of respiration	0/20
HP: 0002795	Functional respiratory abnormality	0/20
HP: 0002813	Abnormality of limb bone morphology	0/20
HP: 0002814	Abnormality of the lower limb	0/20
HP: 0002960	Autoimmunity	0/20
HP: 0003110	Abnormality of urine homeostasis	0/20
HP: 0003272	Abnormality of the hip bone	0/20
HP: 0003613	Antiphospholipid antibody positivity	0/20
HP: 0004364	Abnormal circulating nitrogen compound concentration	0/20
HP: 0004377	Hematological neoplasm	0/20
HP: 0004418	Thrombophlebitis	0/20
HP: 0004936	Venous thrombosis	0/20
HP: 0005526	Lymphoid leukemia	0/20
HP: 0010978	Abnormality of immune system physiology	0/20
HP: 0010987	Abnormal cellular immune system morphology	0/20
HP: 0011277	Abnormality of the urinary system physiology	0/20
HP: 0011793	Neoplasm by anatomical site	0/20
HP: 0011842	Abnormality of skeletal morphology	0/20
HP: 0011844	Abnormal appendicular skeleton morphology	0/20
HP: 0020129	Abnormal urine protein level	0/20
HP: 0030057	Autoimmune antibody positivity	0/20
HP: 0032180	Abnormal circulating metabolite concentration	0/20
HP: 0032251	Abnormal immune system morphology	0/20
HP: 0040064	Abnormality of limbs	0/20
HP: 0040068	Abnormality of limb bone	0/20
HP: 0040069	Abnormal lower limb bone morphology	0/20
HP: 0100724	Hypercoagulability	0/20

Name

Top Correlation

HP: 0000079

Abnormality of the urinary system

0/20

HP: 0000093

Proteinuria

0/20

HP: 0000118

Phenotypic abnormality

0/20

HP: 0000119