Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2227564
rs2227564
0.846 0.179 10 73913343 missense variant T/C snp 0.75 0.79
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.800 1 2012 2012
dbSNP: rs2227564
rs2227564
0.846 0.179 10 73913343 missense variant T/C snp 0.75 0.79
ALZHEIMER DISEASE, LATE-ONSET, SUSCEPTIBILITY TO
0.700 4 2003 2007
dbSNP: rs2227551
rs2227551
0.821 0.107 10 73909432 intron variant G/C,T snp 0.65
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 2 2016 2017
dbSNP: rs2227551
rs2227551
0.821 0.107 10 73909432 intron variant G/C,T snp 0.65
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1 2017 2017
dbSNP: rs2227551
rs2227551
0.821 0.107 10 73909432 intron variant G/C,T snp 0.65
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
Digestive System Diseases 0.700 1 2017 2017
dbSNP: rs2227551
rs2227551
0.821 0.107 10 73909432 intron variant G/C,T snp 0.65
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1 2017 2017
dbSNP: rs2227551
rs2227551
0.821 0.107 10 73909432 intron variant G/C,T snp 0.65
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1 2017 2017
dbSNP: rs2227564
rs2227564
0.846 0.179 10 73913343 missense variant T/C snp 0.75 0.79
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1 2017 2017
dbSNP: rs2227564
rs2227564
0.846 0.179 10 73913343 missense variant T/C snp 0.75 0.79
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Mental Disorders; Nervous System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2227564
rs2227564
0.846 0.179 10 73913343 missense variant T/C snp 0.75 0.79
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2227564
rs2227564
0.846 0.179 10 73913343 missense variant T/C snp 0.75 0.79
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4065
rs4065
0.846 0.071 10 73916706 3 prime UTR variant C/T snp 0.49
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4065
rs4065
0.846 0.071 10 73916706 3 prime UTR variant C/T snp 0.49
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2011 2011
dbSNP: rs4065
rs4065
0.846 0.071 10 73916706 3 prime UTR variant C/T snp 0.49
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4065
rs4065
0.846 0.071 10 73916706 3 prime UTR variant C/T snp 0.49
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2011 2011