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: 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: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
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: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2012 2012
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0221013
Disease: Mastocytosis, Systemic
Mastocytosis, Systemic
0.010 1.000 1 2001 2001
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2014 2014
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis
0.010 1.000 1 2008 2008
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C1276072
Disease: Adult atopic dermatitis
Adult atopic dermatitis
0.010 1.000 1 2000 2000
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
Malignant neoplasm of gastrointestinal tract
0.010 1.000 1 2017 2017
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.010 1.000 1 2016 2016
dbSNP: rs1801275
rs1801275
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2014 2014