Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.850 1.000 5 2011 2019
dbSNP: rs1466535
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		0.840 1.000 1 2011 2015
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.800 1.000 1 2013 2016
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2011 2011
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C0018681
Disease: Headache
Headache 		0.700 1.000 1 2018 2018
dbSNP: rs11172114
rs11172114
LRP1
12 57135660 intron variant C/T snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs1385526
rs1385526
LRP1
1.000 0.040 12 57138966 intron variant G/C snv 0.26
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		0.700 1.000 1 2017 2017
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1 		0.700 1.000 1 2018 2018
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease 		0.700 1.000 1 2018 2018
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs4759277
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs715948
rs715948
LRP1
12 57139199 intron variant T/C snv 0.72
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7398375
rs7398375
LRP1 ; LRP1-AS
0.790 0.080 12 57147065 intron variant C/G snv 0.26
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs7398375
rs7398375
LRP1 ; LRP1-AS
0.790 0.080 12 57147065 intron variant C/G snv 0.26
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs7398375
rs7398375
LRP1 ; LRP1-AS
0.790 0.080 12 57147065 intron variant C/G snv 0.26
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019