Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2018 2018
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0018801
Disease: Heart failure
Heart failure 		0.010 < 0.001 1 2012 2012
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C2826320
Disease: Refractory Neutropenia
Refractory Neutropenia 		0.010 1.000 1 2012 2012
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		0.010 1.000 1 2009 2009
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.010 1.000 1 2002 2002
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 1.000 1 2018 2018
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 		0.010 1.000 1 2009 2009
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.010 < 0.001 1 2018 2018
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2005 2005
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.010 1.000 1 2006 2006
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0392663
Disease: Infection by Wuchereria bancrofti
Infection by Wuchereria bancrofti 		0.010 1.000 1 2011 2011
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2015 2015
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0702166
Disease: Acne
Acne 		0.010 1.000 1 2010 2010
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis 		0.010 1.000 1 2001 2001
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 1.000 1 2018 2018
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 < 0.001 1 2012 2012
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0003864
Disease: Arthritis
Arthritis 		0.010 1.000 1 2004 2004
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0042384
Disease: Vasculitis
Vasculitis 		0.010 1.000 1 2001 2001
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2018 2018
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		0.010 1.000 1 2009 2009
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2003 2003
dbSNP: rs1061622
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2018 2018