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 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.800 1.000 42 2008 2018
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
180 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.800 0.917 13 2011 2016
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
44 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.750 1.000 7 2009 2015
oligodendroglioma
CUI: C0028945
Disease: oligodendroglioma
15 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.750 1.000 6 2013 2015
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
163 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.730 1.000 5 2010 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
215 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.710 1.000 8 2009 2016
GLIOBLASTOMA MULTIFORME, SOMATIC
CUI: C4016231
Disease: GLIOBLASTOMA MULTIFORME, SOMATIC
1 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 3 2008 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
29 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
44 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
226 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
203 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
303 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
66 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
53 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Transitional cell carcinoma of bladder
147 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.700 1 2016 2016
Well Differentiated Oligodendroglioma
16 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.050 1.000 5 2013 2015
Anaplastic astrocytoma
CUI: C0334579
Disease: Anaplastic astrocytoma
6 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.030 1.000 3 2014 2014
Malignant Glioma
CUI: C0555198
Disease: Malignant Glioma
11 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.030 1.000 3 2013 2016
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
127 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.010 1.000 1 2014 2014
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
16 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.010 1.000 1 2016 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 0.010 1.000 1 2015 2015