Source: CLINVAR

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: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome 		0.800 1.000 9 1990 2018
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.710 1.000 1 2016 2017
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.710 1.000 0 2017 2017
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 1.000 5 1994 2011
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0677865
Disease: Brain Stem Glioma
Brain Stem Glioma 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0206686
Disease: Adrenocortical carcinoma
Adrenocortical carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs876660754
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		0.700 1.000 1 2016 2016