rs1061622, TNFRSF1B

N. diseases: 33
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.
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2001 2001
Vasculitis
CUI: C0042384
Disease: Vasculitis
24 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2001 2001
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2002 2002
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2003 2003
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2004 2004
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2005 2005
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2006 2006
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2006 2006
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.040 1.000 4 2000 2009
Hyperandrogenism
CUI: C0206081
Disease: Hyperandrogenism
24 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.020 1.000 2 2002 2009
21-hydroxylase deficiency
CUI: C0852654
Disease: 21-hydroxylase deficiency
28 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2009 2009
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
62 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2009 2009
Deficiency of steroid 21-monooxygenase
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
26 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2009 2009
Acne
CUI: C0702166
Disease: Acne
11 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2010 2010
Acne Vulgaris
CUI: C0001144
Disease: Acne Vulgaris
37 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2010 2010
Infection by Wuchereria bancrofti
CUI: C0392663
Disease: Infection by Wuchereria bancrofti
2 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2011 2011
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2011 2011
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1 2012 2012
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1 2012 2012
Refractory Neutropenia
CUI: C2826320
Disease: Refractory Neutropenia
1 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.070 1.000 7 2004 2015
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.020 1.000 2 2001 2015
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.020 1.000 2 2015 2015