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.
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
Malignant neoplasm of soft tissue
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
32 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2020 2020
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
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
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 cholangiocarcinoma of intrahepatic biliary tract
CUI: C4284013
Disease: Primary cholangiocarcinoma of intrahepatic biliary tract
10 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2018 2018
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
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2020 2020
Secondary malignant neoplasm of lung
CUI: C0153676
Disease: 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
Sinonasal undifferentiated carcinoma
CUI: C1710096
Disease: Sinonasal undifferentiated carcinoma
8 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2019 2019
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
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
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.710 1.000 2 2016 2017
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.710 1.000 2 2012 2016
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
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
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.020 1.000 2 2009 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.020 1.000 2 2018 2019
melanoma
CUI: C0025202
Disease: melanoma
515 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.020 1.000 2 2010 2018
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
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.060 1.000 6 2009 2019