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: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2009 2013
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 1997 2014
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2010 2012
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 1997 2014
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2012 2012
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2007 2007
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2019 2019
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2018 2018
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
Slow acetylator due to N-acetyltransferase enzyme variant
0.010 1.000 1 2006 2006
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.010 1.000 1 2017 2017
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C3203670
Disease: NAT2 polymorphism
NAT2 polymorphism
0.010 1.000 1 2012 2012
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0029172
Disease: Oral Submucous Fibrosis
Oral Submucous Fibrosis
0.010 1.000 1 2012 2012
dbSNP: rs1799931
rs1799931
0.742 0.320 8 18400860 missense variant G/A snv 5.8E-02 3.9E-02
CUI: C0021364
Disease: Male infertility
Male infertility
0.010 1.000 1 2014 2014