rs6679677, PHTF1

N. diseases: 26
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.
Diabetes Mellitus, Insulin-Dependent
954 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.810 1.000 5 2007 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 4 2015 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.800 1.000 4 2007 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.800 1.000 3 2008 2015
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.710 1.000 2 2012 2015
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 2 2015 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.710 1.000 2 2015 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
76 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
Common Variable Immunodeficiency
CUI: C0009447
Disease: Common Variable Immunodeficiency
85 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.800 1.000 1 2012 2012
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
Juvenile pauciarticular chronic arthritis
31 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2013 2013
Juvenile-Onset Still Disease
CUI: C0087031
Disease: Juvenile-Onset Still Disease
41 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2011 2011
Myositis
CUI: C0027121
Disease: Myositis
43 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2019 2019
Oligoarticular Juvenile Idiopathic Arthritis
35 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.800 1.000 1 2013 2013
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
31 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2013 2013
Rheumatoid Arthritis, Systemic Juvenile
42 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2013 2013
Systemic onset juvenile chronic arthritis
53 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2013 2013
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2019 2019
Temporal Arteritis
CUI: C1956391
Disease: Temporal Arteritis
6 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015