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.
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
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
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
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
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
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
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
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
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
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
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
30 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
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
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
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
32 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2018 2018
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Brain Stem Glioma
CUI: C0677865
Disease: Brain Stem Glioma
45 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.605 0.520 2 208248389 missense variant G/A;C;T snv 0.010 1.000 1 2018 2018
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
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
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
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