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: rs1056628
rs1056628
20 46016407 3 prime UTR variant A/C snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2018 2018
dbSNP: rs1056628
rs1056628
20 46016407 3 prime UTR variant A/C snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs13925
rs13925
1.000 0.080 20 46016326 synonymous variant G/A snv 0.15 0.15
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2018 2018
dbSNP: rs139620474
rs139620474
1.000 0.120 20 46009878 missense variant C/A;T snv 1.9E-05 7.7E-05
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2002 2002
dbSNP: rs1430059719
rs1430059719
1.000 0.080 20 46012456 missense variant G/C snv 4.0E-06
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.010 1.000 1 2006 2006
dbSNP: rs1459997671
rs1459997671
0.882 0.120 20 46010963 synonymous variant C/T snv
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2013 2013
dbSNP: rs1459997671
rs1459997671
0.882 0.120 20 46010963 synonymous variant C/T snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.010 1.000 1 2009 2009
dbSNP: rs1459997671
rs1459997671
0.882 0.120 20 46010963 synonymous variant C/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2005 2005
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease
0.010 1.000 1 2014 2014
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis
0.010 1.000 1 2018 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 < 0.001 1 2018 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.010 1.000 1 2008 2008
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2009 2009
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 1.000 1 2009 2009
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C1443892
Disease: Chronic Q Fever
Chronic Q Fever
0.010 1.000 1 2017 2017
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.010 1.000 1 2018 2018
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome
0.010 1.000 1 2010 2010
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C2721603
Disease: Henoch-Schonlein purpura nephritis
Henoch-Schonlein purpura nephritis
0.010 1.000 1 2016 2016
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2010 2010
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
0.010 1.000 1 2015 2015
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2010 2010
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0024031
Disease: Low Back Pain
Low Back Pain
0.010 1.000 1 2017 2017
dbSNP: rs17576
rs17576
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36
CUI: C0877015
Disease: Pelvic Organ Prolapse
Pelvic Organ Prolapse
0.010 1.000 1 2010 2010