rs8099917, None

N. diseases: 60
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.
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 0.500 2 2012 2012
Acute hepatitis C
CUI: C0400914
Disease: Acute hepatitis C
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Anemia
CUI: C0002871
Disease: Anemia
94 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Congenital hypoplasia of adrenal gland
13 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
X-linked Adrenal Hypoplasia
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
70 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Hemophilia, NOS
CUI: C0684275
Disease: Hemophilia, NOS
8 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Human immunodeficiency virus (HIV) II infection category B1
56 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Sensory neuropathy
CUI: C0151313
Disease: Sensory neuropathy
15 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Chronic hepatitis C virus genotype 1
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2014
Recurrent hepatitis
CUI: C3887641
Disease: Recurrent hepatitis
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2014
Chronic hepatitis C genotype 4
CUI: C4049431
Disease: Chronic hepatitis C genotype 4
3 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Hepatitis D Infection
CUI: C0011226
Disease: Hepatitis D Infection
4 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Hepatitis D, Chronic
CUI: C0524911
Disease: Hepatitis D, Chronic
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
HTLV-I Infections
CUI: C0020097
Disease: HTLV-I Infections
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Infectious Mononucleosis
CUI: C0021345
Disease: Infectious Mononucleosis
4 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Influenza
CUI: C0021400
Disease: Influenza
17 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
TROPICAL CALCIFIC PANCREATITIS
CUI: C1842402
Disease: TROPICAL CALCIFIC PANCREATITIS
13 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Tropical Spastic Paraparesis
CUI: C0030481
Disease: Tropical Spastic Paraparesis
4 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2014 2014
Cryoglobulinemia
CUI: C0010403
Disease: Cryoglobulinemia
7 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2015 2015
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2015 2015
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2015 2015
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2016