rs371409680, TP53

N. diseases: 10
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.700 1.000 10 1998 2015
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.700 0
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.700 0
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.020 1.000 2 2002 2005
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.010 1.000 1 2002 2002
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.010 1.000 1 2002 2002
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.010 1.000 1 2002 2002
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.010 1.000 1 2002 2002
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.010 1.000 1 2002 2002
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 0.010 1.000 1 2002 2002