Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
124 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.020 1.000 2 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.020 1.000 2 2014 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.020 1.000 2 2014 2015
HIV Infections
CUI: C0019693
Disease: HIV Infections
54 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.020 1.000 2 2011 2016
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
26 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2011 2011
Schwartz-Jampel Syndrome
CUI: C0036391
Disease: Schwartz-Jampel Syndrome
7 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2014 2014
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1 2011 2011
Toxic Epidermal Necrolysis
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
17 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2014 2014
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
37 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2006 2006
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
60 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2007 2007
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
53 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2011 2011
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
113 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2007 2007
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
16 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1 2011 2011
Neurologic Symptoms
CUI: C0235031
Disease: Neurologic Symptoms
11 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1.000 1 2005 2005
leukemia
CUI: C0023418
Disease: leukemia
76 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1 2011 2011
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
99 0.744 0.393 19 41006936 missense variant G/A,T snp 4.0E-06; 0.27 0.26 0.010 1 2011 2011