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: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2013 2015
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.020 1.000 2 2014 2015
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.020 1.000 2 2015 2019
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma
0.010 1.000 1 2008 2008
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura
0.010 1.000 1 2017 2017
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
0.010 1.000 1 2013 2013
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2011 2011
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
0.010 1.000 1 2017 2017
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2018 2018
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2017 2017
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.010 1.000 1 2019 2019
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2009 2009
dbSNP: rs1927914
rs1927914
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.020 1.000 2 2019 2019
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0085166
Disease: Bacterial Vaginosis
Bacterial Vaginosis
0.010 1.000 1 2008 2008
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0032927
Disease: Precancerous Conditions
Precancerous Conditions
0.010 1.000 1 2019 2019
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 < 0.001 1 2016 2016
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2007 2007
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
0.010 1.000 1 2016 2016
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura
0.010 1.000 1 2017 2017
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.010 1.000 1 2019 2019
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2015 2015