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: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
0.800 1.000 10 1994 2015
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 7 1994 2015
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0677865
Disease: Brain Stem Glioma
Brain Stem Glioma
0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.700 0