rs597808, ATXN2

N. diseases: 19
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 2 2019 2019
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2019 2019
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2018 2018
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2018 2018
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2019 2019
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
52 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2019 2019
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2018 2018
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2015 2015
Smoking
CUI: C0037369
Disease: Smoking
765 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2019 2019
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2018 2018
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.742 0.200 12 111535554 intron variant A/G snv 0.67 0.700 1.000 1 2019 2019