I87.1

Case	Control
186	460019

Case

Control

186

460019

Top SNP Information

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds Ratio
chr11:110587966	rs117201290	-	G>C	14	9100	28.32	1.029e-07	3.845
chr2:115250149	rs115087919	DPP10	G>A	15	10850	26.06	3.309e-07	3.525
chr1:193024643	rs77333031	UCHL5	C>T	37	41753	25.0	5.721e-07	2.314
chr14:90528797	rs7157583	KCNK13	G>A	16	12241	25.0	5.742e-07	3.33
chr11:108711110	rs79573524	DDX10	A>G	28	28285	24.6	7.07e-07	2.555
chr1:192952704	rs79421289	-	G>A	36	40822	24.07	9.306e-07	2.302
chr11:110307019	rs116914612	FDX1	A>G	17	13820	23.73	1.11e-06	3.143
chr20:46660391	rs116958724	-	C>T	20	17887	23.19	1.466e-06	2.876
chr10:97209774	rs61868672	SORBS1	G>A	37	43087	23.16	1.492e-06	2.247
chr5:127078312	rs115309353	CCDC192	A>G	19	16588	22.91	1.698e-06	2.927
chr8:96551531	rs117575926	-	G>A	16	12838	22.83	1.769e-06	3.174
chr1:177896795	rs593809	SEC16B	A>C	47	60210	22.68	1.911e-06	2.065
chr2:208914389	rs74720175	-	C>T	19	16684	22.64	1.954e-06	2.91
chr5:27209087	rs12519381	-	T>A	15	11740	22.59	2.002e-06	3.262
chr7:117177013	rs17449134	CFTR	G>A	31	33860	22.48	2.127e-06	2.365
chr3:125822997	rs115050642	ALDH1L1	G>A	19	16923	22.44	2.167e-06	2.898
chr11:78204073	rs66546995	NARS2	C>CACAGAT	105	174494	22.11	2.58e-06	1.701
chr11:78214673	rs10128743	NARS2	C>T	108	178047	21.97	2.769e-06	1.688
chr10:8099823	rs10905278	GATA3	G>A	44	55773	21.62	3.33e-06	2.07
chr15:59263452	rs62002477	RNF111	G>C	21	19781	21.5	3.547e-06	2.714

Associated Phenotypes ^ⓘ

ID	Name	Top Correlation
HP: 0012151	Hemothorax	1/20
HP: 0025491	Venous stenosis	2/20

Name

Top Correlation

1/20

2/20

ID	Name	Top Correlation
HP: 0000118	Phenotypic abnormality	0/20
HP: 0000152	Abnormality of head or neck	0/20
HP: 0000234	Abnormality of the head	0/20
HP: 0000271	Abnormality of the face	0/20
HP: 0000478	Abnormality of the eye	0/20
HP: 0000479	Abnormal retinal morphology	0/20
HP: 0000504	Abnormality of vision	0/20
HP: 0000505	Visual impairment	0/20
HP: 0000707	Abnormality of the nervous system	0/20
HP: 0000969	Edema	0/20
HP: 0001098	Abnormal fundus morphology	0/20
HP: 0001103	Abnormal macular morphology	0/20
HP: 0001123	Visual field defect	0/20
HP: 0001133	Constriction of peripheral visual field	0/20
HP: 0001626	Abnormality of the cardiovascular system	0/20
HP: 0001871	Abnormality of blood and blood-forming tissues	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: 0002088	Abnormal lung morphology	0/20
HP: 0002103	Abnormality of the pleura	0/20
HP: 0002597	Abnormality of the vasculature	0/20
HP: 0002624	Abnormal venous morphology	0/20
HP: 0004329	Abnormal posterior eye segment morphology	0/20
HP: 0004417	Intermittent claudication	0/20
HP: 0004936	Venous thrombosis	0/20
HP: 0008046	Abnormal retinal vascular morphology	0/20
HP: 0008047	Abnormality of the vasculature of the eye	0/20
HP: 0011025	Abnormal cardiovascular system physiology	0/20
HP: 0011032	Abnormality of fluid regulation	0/20
HP: 0012252	Abnormal respiratory system morphology	0/20
HP: 0012337	Abnormal homeostasis	0/20
HP: 0012372	Abnormal eye morphology	0/20
HP: 0012373	Abnormal eye physiology	0/20
HP: 0012531	Pain	0/20
HP: 0012636	Retinal vein occlusion	0/20
HP: 0012639	Abnormal nervous system morphology	0/20
HP: 0020165	Branch retinal vein occlusion	0/20
HP: 0020166	Central retinal vein occlusion	0/20
HP: 0025015	Abnormal vascular morphology	0/20
HP: 0025142	Constitutional symptom	0/20
HP: 0025323	Abnormal arterial physiology	0/20
HP: 0030163	Abnormal vascular physiology	0/20
HP: 0030242	Portal vein thrombosis	0/20
HP: 0030247	Splanchnic vein thrombosis	0/20
HP: 0030498	Macular thickening	0/20
HP: 0030680	Abnormality of cardiovascular system morphology	0/20
HP: 0040049	Macular edema	0/20
HP: 0410019	Epigastric pain	0/20

Name

Top Correlation

HP: 0000118

Phenotypic abnormality

0/20

HP: 0000152

Abnormality of head or neck

0/20

HP: 0000234

Abnormality of the head

0/20

HP: 0000271