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: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.020 0.500 2 2011 2013
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
0.010 < 0.001 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C1328504
Disease: Hormone refractory prostate cancer
Hormone refractory prostate cancer
0.010 1.000 1 2013 2013
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0023530
Disease: Leukopenia
Leukopenia
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C2347126
Disease: Microscopic Polyarteritis
Microscopic Polyarteritis
0.010 1.000 1 2020 2020
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0027947
Disease: Neutropenia
Neutropenia
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0023895
Disease: Liver diseases
Liver diseases
0.010 1.000 1 2013 2013
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
0.010 1.000 1 2015 2015
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2017 2017
dbSNP: rs4149117
rs4149117
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 1.000 1 2017 2017