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: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C1840254
Disease: ATOPY, SUSCEPTIBILITY TO (finding)
ATOPY, SUSCEPTIBILITY TO (finding)
0.700 0
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0004096
Disease: Asthma
Asthma
0.100 1.000 13 2002 2016
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0017638
Disease: Glioma
Glioma
0.050 1.000 5 2011 2016
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.040 0.750 4 2006 2019
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.040 0.750 4 2006 2013
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.030 1.000 3 2005 2013
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.020 1.000 2 2014 2014
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.020 0.500 2 2001 2014
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0013595
Disease: Eczema
Eczema
0.020 < 0.001 2 2013 2014
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.020 < 0.001 2 2005 2011
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.020 1.000 2 2007 2013
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2007 2013
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 < 0.001 1 2001 2001
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
0.010 1.000 1 2015 2015
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0333307
Disease: Superficial ulcer
Superficial ulcer
0.010 1.000 1 2010 2010
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.010 < 0.001 1 2018 2018
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C4025886
Disease: Severe periodontitis
Severe periodontitis
0.010 1.000 1 2011 2011
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2007 2007
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2007 2007
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0011603
Disease: Dermatitis
Dermatitis
0.010 < 0.001 1 2014 2014
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization
0.010 1.000 1 2009 2009
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial
0.010 1.000 1 2015 2015
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
0.010 1.000 1 2007 2007
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
0.010 1.000 1 2007 2007