Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.060 0.833 6 2010 2019
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		0.020 1.000 2 2005 2010
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		0.020 1.000 2 2014 2016
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2019 2019
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0035412
Disease: Rhabdomyosarcoma
Rhabdomyosarcoma 		0.010 1.000 1 2018 2018
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0028945
Disease: oligodendroglioma
oligodendroglioma 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		0.010 1.000 1 2015 2015
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2006 2006
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0751396
Disease: Well Differentiated Oligodendroglioma
Well Differentiated Oligodendroglioma 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2015 2015
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0206696
Disease: Carcinoma, Signet Ring Cell
Carcinoma, Signet Ring Cell 		0.010 1.000 1 2016 2016
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma 		0.010 1.000 1 2018 2018
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0205697
Disease: Carcinoma, Spindle-Cell
Carcinoma, Spindle-Cell 		0.010 1.000 1 2015 2015
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0086692
Disease: Benign Neoplasm
Benign Neoplasm 		0.010 1.000 1 2012 2012
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0279070
Disease: Adult Oligodendroglioma
Adult Oligodendroglioma 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs1131691021
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0279612
Disease: Childhood Embryonal Rhabdomyosarcoma
Childhood Embryonal Rhabdomyosarcoma 		0.010 1.000 1 2018 2018