rs1024611, None

N. diseases: 63
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.
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
1 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.700 0
CORONARY ARTERY DISEASE, MODIFIER OF
1 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.700 0
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)
3 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.700 0
SPINA BIFIDA, SUSCEPTIBILITY TO
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
1 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.700 0
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.030 1.000 3 2014 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.030 0.667 3 2010 2015
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.020 1.000 2 2016 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.020 1.000 2 2016 2018
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.020 1.000 2 2017 2019
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.020 1.000 2 2014 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.020 1.000 2 2013 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2018 2018
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2020 2020
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2014 2014
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2012 2012
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2015 2015
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2014 2014
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2010 2010
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2019 2019