rs57095329, MIR3142HG

N. diseases: 25
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.030 1.000 3 2011 2016
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.020 1.000 2 2015 2016
Seizures
CUI: C0036572
Disease: Seizures
553 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.020 1.000 2 2015 2016
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2019 2019
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2019 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2014 2014
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2016 2016
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2019 2019
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2017 2017
Creutzfeldt-Jakob Disease, Sporadic
CUI: C1852467
Disease: Creutzfeldt-Jakob Disease, Sporadic
23 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2018 2018
Drug Resistant Epilepsy
CUI: C1096063
Disease: Drug Resistant Epilepsy
35 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2015 2015
Fatal Familial Insomnia
CUI: C0206042
Disease: Fatal Familial Insomnia
16 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2018 2018
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2014 2014
Juvenile rheumatoid arthritis
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
10 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1 2019 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2020 2020
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2014 2014
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2015 2015
Mutism
CUI: C0026884
Disease: Mutism
4 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2018 2018
Myoclonus
CUI: C0027066
Disease: Myoclonus
34 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2018 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2020 2020
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2016 2016
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2014 2014
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2014 2014
Severe Sepsis
CUI: C1719672
Disease: Severe Sepsis
29 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 0.010 1.000 1 2014 2014