Source: ALL

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: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO (finding)
0.700 0
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0.700 0
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CORONARY ARTERY DISEASE, MODIFIER OF
0.700 0
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2014 2019
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.030 0.667 3 2010 2015
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.020 1.000 2 2016 2018
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.020 1.000 2 2016 2018
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.020 1.000 2 2014 2014
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.020 1.000 2 2017 2019
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 1.000 2 2013 2016
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2015 2015
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2017 2017
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.010 1.000 1 2014 2014
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2019 2019
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 1.000 1 2015 2015
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.010 1.000 1 2007 2007
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.010 1.000 1 2014 2014
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0014057
Disease: Japanese Encephalitis
Japanese Encephalitis
0.010 1.000 1 2019 2019
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2016 2016
dbSNP: rs1024611
rs1024611
0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.010 1.000 1 2019 2019