rs121913500, IDH1

N. diseases: 96
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 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.040 0.750 4 2014 2018
Childhood Ependymoma
CUI: C1851584
Disease: Childhood Ependymoma
3 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2014 2014
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.100 1.000 18 2011 2019
Childhood Gliomatosis Cerebri
CUI: C3897070
Disease: Childhood Gliomatosis Cerebri
6 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2011 2012
Childhood Oligoastrocytoma
CUI: C3899649
Disease: Childhood Oligoastrocytoma
3 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2012 2017
Childhood Oligodendroglioma
CUI: C0280475
Disease: Childhood Oligodendroglioma
19 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.080 1.000 8 2012 2019
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Childhood Pleomorphic Xanthoastrocytoma
CUI: C3899645
Disease: Childhood Pleomorphic Xanthoastrocytoma
7 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2016 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
Diffuse Astrocytoma
CUI: C0280785
Disease: Diffuse Astrocytoma
8 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.030 1.000 3 2013 2018
Diffuse Glioma
CUI: C4289690
Disease: Diffuse Glioma
7 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.040 0.750 4 2012 2019
Enchondroma
CUI: C1704356
Disease: Enchondroma
13 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2011 2018
Ependymoma
CUI: C0014474
Disease: Ependymoma
8 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2014 2014
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2018 2018
Epileptic Seizures
CUI: C4317109
Disease: Epileptic Seizures
7 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.800 0.977 43 2010 2020
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.100 0.969 32 2009 2020
GLIOBLASTOMA MULTIFORME, SOMATIC
CUI: C4016231
Disease: GLIOBLASTOMA MULTIFORME, SOMATIC
1 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.700 0
Glioblastoma, IDH-Mutant
CUI: C1519214
Disease: Glioblastoma, IDH-Mutant
4 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.030 0.667 3 2012 2018
Glioblastoma, IDH-Wildtype
CUI: C1514422
Disease: Glioblastoma, IDH-Wildtype
4 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2020 2020
Glioma
CUI: C0017638
Disease: Glioma
353 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 49 2009 2019
Gliomatosis cerebri
CUI: C0334576
Disease: Gliomatosis cerebri
6 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.020 1.000 2 2011 2012
Glioneuronal Tumor with Neuropil-Like Islands
CUI: C2985171
Disease: Glioneuronal Tumor with Neuropil-Like Islands
1 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2012 2012