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.
Glioma
CUI: C0017638
Disease: Glioma
180 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.730 1.000 5 2008 2014
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.720 1.000 9 2009 2016
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
44 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.720 1.000 4 2009 2015
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
53 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.710 1.000 2 2012 2016
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.710 1.000 1 2015 2015
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
66 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
226 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
44 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
163 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Transitional cell carcinoma of bladder
147 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
29 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
303 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
203 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
180 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.700 1 2016 2016
Hemangioma
CUI: C0018916
Disease: Hemangioma
6 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.020 1.000 2 2012 2014
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
42 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.010 1.000 1 2009 2009
Clear Cell Hepatocellular Carcinoma
CUI: C1333067
Disease: Clear Cell Hepatocellular Carcinoma
1 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.010 1.000 1 2017 2017
Vascular lesions
CUI: C1402315
Disease: Vascular lesions
4 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.010 1.000 1 2012 2012
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
61 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.010 1.000 1 2016 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
364 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.010 1.000 1 2016 2016
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
87 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.010 1.000 1 2009 2009