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.
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
Acute infectious disease
CUI: C0275518
Disease: Acute infectious disease
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1 2017 2017
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
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1 2017 2017
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
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
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Congenital Bleeding Disorder
CUI: C3641106
Disease: Congenital Bleeding Disorder
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Congenital hypoplasia of adrenal gland
CUI: C0220766
Disease: 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
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
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
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2016 2016
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
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
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
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: 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
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