Chest pain

0100749

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

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Interactive Plot

Statistics

Case	Control
58963	401231

Phenotype Definition

An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the chest. []

Top SNP Information

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr5:33951693	rs16891982	SLC45A2	G>C	9976	57082	226.7	3.083e-51	1.185
chr5:33958959	rs28777	SLC45A2	A>C	8486	48506	193.4	5.655e-44	1.184
chr5:33955673	rs35391	SLC45A2	C>T	6134	34846	148.4	3.969e-34	1.188
chr5:33955326	rs35390	SLC45A2	A>C	6155	34992	147.3	6.756e-34	1.187
chr6:161010118	rs10455872	LPA	A>G	10576	63123	130.5	3.152e-30	1.133
chr9:22115959	rs2383207	-	G>A	58121	403918	129.3	5.833e-30	0.9336
chr5:33951116	rs35397	SLC45A2	T>G	12782	77326	126.1	2.902e-29	1.12
chr6:160997118	rs74617384	LPA	A>T	10275	61552	119.6	7.726e-28	1.129
chr9:22124477	rs10757278	-	A>G	62333	403767	116.3	4.017e-27	1.067
chr9:22096055	rs10757274	-	A>G	63155	409397	114.4	1.047e-26	1.067
chr9:22081850	rs6475606	-	C>T	64674	419595	114.3	1.145e-26	1.067
chr9:22098574	rs4977574	-	A>G	62864	407557	113.7	1.479e-26	1.066
chr9:22088260	rs10757272	-	C>T	63038	408710	113.2	1.936e-26	1.066
chr9:22125347	rs1333048	-	A>C	64558	419099	112.0	3.489e-26	1.066
chr9:22125503	rs1333049	-	G>C	62334	404104	109.2	1.479e-25	1.065
chr2:210564805	rs13424278	MAP2	A>G	2658	14355	106.4	6.097e-25	1.246
chr6:160608804	rs16891156	SLC22A2	A>C	3554	19809	104.9	1.296e-24	1.208
chr1:110689011	rs76894936	-	C>A	2306	12412	95.0	1.907e-22	1.249
chr2:210484445	rs2663644	MAP2	G>A	3052	16942	90.51	1.838e-21	1.208
chr23:102191083	rs5987498	-	G>T	2228	13046	85.02	2.952e-20	1.238
chr6:161010118	rs10455872	LPA	A>G	10411	62339	158.4	2.54e-36	1.15
chr6:160997118	rs74617384	LPA	A>T	10110	60778	145.4	1.75e-33	1.145
chr9:22124477	rs10757278	-	A>G	58644	385462	117.7	1.997e-27	1.07
chr9:22096055	rs10757274	-	A>G	59391	390762	114.6	9.631e-27	1.069
chr9:22098574	rs4977574	-	A>G	59194	389532	114.0	1.327e-26	1.069
chr9:22125503	rs1333049	-	G>C	58591	385327	112.7	2.454e-26	1.069
chr9:22088260	rs10757272	-	C>T	58995	388211	112.3	3.034e-26	1.068
chr9:22115959	rs2383207	-	G>A	55458	390563	110.4	7.939e-26	0.9364
chr9:22125347	rs1333048	-	A>C	60479	398662	109.2	1.501e-25	1.067
chr9:22081850	rs6475606	-	C>T	58526	386236	92.69	6.116e-22	1.062
chr6:160848743	rs9457925	SLC22A3	G>A	2587	14458	87.1	1.033e-20	1.223
chr6:160961137	rs3798220	LPA	T>C	2543	14239	83.73	5.682e-20	1.22
chr6:160922870	rs117733303	-	A>G	2568	14416	82.66	9.767e-20	1.217
chr6:160608804	rs16891156	SLC22A2	A>C	2794	15905	77.54	1.302e-18	1.2
chr6:160687412	rs10080815	SLC22A2	T>G	2707	15430	74.03	7.713e-18	1.199
chr9:22083404	rs1333040	-	T>C	47418	333140	71.88	2.285e-17	0.9475
chr9:22003223	rs3217992	AL359922.1	C>T	44278	291972	60.85	6.159e-15	1.052
chr9:22068652	rs4977756	-	A>G	46029	322611	58.36	2.181e-14	0.9523
chr9:22033366	rs2157719	-	T>C	49831	348391	56.67	5.16e-14	0.9536
chr9:22043926	rs1412829	-	A>G	48340	338106	55.49	9.395e-14	0.9538

Location	SNP	Gene	Ref>Alt	Alt in Case	Alt in Control	Chi-square	P-value	Odds ratio
chr6:161010118	rs10455872	LPA	A>G	10411	26913	153.8	2.588e-35	1.161
chr6:160997118	rs74617384	LPA	A>T	10110	26226	142.5	7.474e-33	1.157
chr9:22124477	rs10757278	-	A>G	58644	167267	127.6	1.382e-29	1.079
chr9:22115959	rs2383207	-	G>A	55458	170995	122.2	2.109e-28	0.9281
chr9:22125503	rs1333049	-	G>C	58591	167236	121.2	3.449e-28	1.077
chr9:22096055	rs10757274	-	A>G	59391	169657	120.9	4.027e-28	1.077
chr9:22098574	rs4977574	-	A>G	59194	169147	119.6	7.778e-28	1.077
chr9:22088260	rs10757272	-	C>T	58995	168580	117.5	2.209e-27	1.076
chr9:22125347	rs1333048	-	A>C	60479	173034	117.4	2.3e-27	1.076
chr9:22081850	rs6475606	-	C>T	58526	167744	97.77	4.703e-23	1.069
chr9:22083404	rs1333040	-	T>C	47418	145614	73.3	1.111e-17	0.9429
chr6:160848743	rs9457925	SLC22A3	G>A	2587	6327	69.84	6.431e-17	1.217
chr6:160961137	rs3798220	LPA	T>C	2543	6228	67.48	2.128e-16	1.215
chr6:160922870	rs117733303	-	A>G	2568	6302	67.04	2.662e-16	1.213
chr6:160687412	rs10080815	SLC22A2	T>G	2707	6713	63.23	1.837e-15	1.201
chr9:22003223	rs3217992	AL359922.1	C>T	44278	126849	62.11	3.247e-15	1.057
chr9:22068652	rs4977756	-	A>G	46029	140951	59.62	1.151e-14	0.9481
chr9:22033366	rs2157719	-	T>C	49831	152158	57.01	4.34e-14	0.9498
chr6:160608804	rs16891156	SLC22A2	A>C	2794	7029	55.49	9.37e-14	1.183
chr9:22031005	rs7865618	-	A>G	49796	151892	54.4	1.635e-13	0.951

Associated Diseases ^ⓘ

ID	Name	Top Correlation
ICD: I200	Unstable angina	15/20
ICD: I208	Other forms of angina pectoris	9/20
ICD: I209	Angina pectoris, unspecified	11/20
ICD: I219	Acute myocardial infarction, unspecified	10/20
ICD: I259	Chronic ischaemic heart disease, unspecified	11/20
ICD: R072	Precordial pain	2/20
ICD: R073	Other chest pain	2/20
ICD: R074	Chest pain, unspecified	5/20
ICD: T828	Other complications of cardiac and vascular prosthetic devices, implants and grafts	11/20

ID	Name	Top Correlation
ICD-10: C781	Secondary malignant neoplasm of mediastinum	0/20
ICD-10: I201	Angina pectoris with documented spasm	0/20
ICD-10: I249	Acute ischaemic heart disease, unspecified	0/20
ICD-10: M940	Chondrocostal junction syndrome [Tietze]	0/20
ICD-10: R071	Chest pain on breathing	0/20

Chest pain

0100749

Normal Case/Contol ⓘ

Sibling Case/Control ⓘ

Links

Statistics

Phenotype Definition

Top SNP Information Show Normal Table Show Sibling SNP

Associated Diseases ⓘ Shared SNP diseases No shared SNP diseases

Normal Case/Contol ^ⓘ

Sibling Case/Control ^ⓘ

Top SNP Information

Associated Diseases ^ⓘ