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: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 2 2018 2019
dbSNP: rs11065898
rs11065898
1.000 0.040 12 111424771 intron variant C/T snv 0.21
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2013 2013
dbSNP: rs3803170
rs3803170
12 111409936 intron variant A/G snv 0.38
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs540639423
rs540639423
12 111407152 intron variant C/T snv 4.6E-03
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.700 1.000 1 2016 2016
dbSNP: rs540639423
rs540639423
12 111407152 intron variant C/T snv 4.6E-03
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.700 1.000 1 2016 2016
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2016 2016
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs7310615
rs7310615
0.882 12 111427245 intron variant C/G snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 10 2009 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 5 2009 2018
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 4 2015 2019
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
Malignant neoplasm of large intestine
0.700 1.000 4 2015 2019