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: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;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: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma 		0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016