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: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
Diarrhoea predominant irritable bowel syndrome
0.010 1.000 1 2011 2011
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2005 2005
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer
0.010 1.000 1 2008 2008
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C1261473
Disease: Sarcoma
Sarcoma
0.010 1.000 1 2012 2012
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2017 2017
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C4551687
Disease: Sarcoma of soft tissue
Sarcoma of soft tissue
0.010 1.000 1 2012 2012
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
Well Differentiated Pancreatic Endocrine Tumor
0.010 1.000 1 2012 2012
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0746883
Disease: Febrile Neutropenia
Febrile Neutropenia
0.010 1.000 1 2014 2014
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2017 2017
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2006 2006
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.010 1.000 1 2015 2015
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2017 2017
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0013537
Disease: Eclampsia
Eclampsia
0.010 < 0.001 1 2011 2011
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0585362
Disease: Squamous cell carcinoma of mouth
Squamous cell carcinoma of mouth
0.010 1.000 1 2012 2012
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
Pituitary-dependent Cushing's disease
0.010 1.000 1 2010 2010
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2013 2013
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2006 2006
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
Squamous cell carcinoma of oropharynx
0.010 1.000 1 2015 2015
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0206754
Disease: Neuroendocrine Tumors
Neuroendocrine Tumors
0.010 1.000 1 2016 2016
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2017 2017
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2018 2018
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2008 2008