rs121913499, IDH1

N. diseases: 51
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.
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2009 2009
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2010 2010
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2010 2010
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2010 2010
Secondary malignant neoplasm of lung
20 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2010 2010
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.020 1.000 2 2009 2011
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2011 2011
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2011 2011
Enchondroma
CUI: C1704356
Disease: Enchondroma
13 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2011 2011
Vascular lesions
CUI: C1402315
Disease: Vascular lesions
9 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2011 2011
Glioma
CUI: C0017638
Disease: Glioma
353 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.720 1.000 2 2011 2012
Adult Fibrosarcoma
CUI: C0278595
Disease: Adult Fibrosarcoma
9 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2012 2012
Chondrosarcoma
CUI: C0008479
Disease: Chondrosarcoma
8 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2012 2012
Fibrosarcoma
CUI: C0016057
Disease: Fibrosarcoma
9 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2012 2012
Hemangioma
CUI: C0018916
Disease: Hemangioma
24 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.020 1.000 2 2011 2013
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2013 2013
Neoplasms, Vascular Tissue
CUI: C0027668
Disease: Neoplasms, Vascular Tissue
1 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2013 2013
Spindle cell hemangioma
CUI: C1304508
Disease: Spindle cell hemangioma
10 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2013 2013
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.720 1.000 4 2009 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.710 1.000 1 2014 2014
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.740 1.000 10 2009 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.710 1.000 2 2011 2016