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.
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
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
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2018 2018
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
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
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
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
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
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2015 2015
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
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
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2018 2018
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2018 2018
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
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
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
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
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1 2018 2018
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
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2018 2018
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
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
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
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