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: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 < 0.001 1 2005 2005
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 < 0.001 1 2005 2005
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 < 0.001 1 2005 2005
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0155877
Disease: Allergic asthma
Allergic asthma
0.010 1.000 1 2006 2006
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
0.010 1.000 1 2006 2006
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 1.000 2 2005 2007
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2007 2007
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 1.000 1 2009 2009
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2011 2011
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 1.000 1 2012 2012
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0018621
Disease: Hay fever
Hay fever
0.010 1.000 1 2012 2012
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 < 0.001 1 2012 2012
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 1.000 3 2010 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
Stage III Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
Stage IIB Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
Stage IIA Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
Stage 0 Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C4525305
Disease: Stage IV Gallbladder Cancer AJCC v8
Stage IV Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2015 2015
dbSNP: rs17577
rs17577
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
0.010 1.000 1 2016 2016