Source: BEFREE

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: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2017 2017
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0.010 1.000 1 2007 2007
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0004936
Disease: Mental disorders
Mental disorders 		0.010 1.000 1 2007 2007
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		0.010 1.000 1 2010 2010
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma 		0.010 1.000 1 2006 2006
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.010 1.000 1 2006 2006
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		0.010 1.000 1 2006 2006
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis 		0.010 1.000 1 2012 2012
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma 		0.010 1.000 1 2006 2006
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2007 2007
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.010 1.000 1 2010 2010
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2012 2012
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0024299
Disease: Lymphoma
Lymphoma 		0.010 1.000 1 2006 2006
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 < 0.001 1 2017 2017
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0155877
Disease: Allergic asthma
Allergic asthma 		0.010 1.000 1 2010 2010
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma 		0.010 1.000 1 2006 2006
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary 		0.010 1.000 1 2012 2012
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		0.010 1.000 1 2005 2005
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2012 2012
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2009 2009
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0013882
Disease: Elephantiasis
Elephantiasis 		0.010 1.000 1 2019 2019
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2009 2009
dbSNP: rs3135932
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11
CUI: C0013884
Disease: Filarial Elephantiases
Filarial Elephantiases 		0.010 1.000 1 2019 2019