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: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0677865
Disease: Brain Stem Glioma
Brain Stem Glioma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
Papillary renal cell carcinoma, sporadic
0.700 1.000 1 2016 2016
dbSNP: rs1057520002
rs1057520002
0.695 0.360 17 7674242 missense variant A/C;G snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.700 0