rs1799930, NAT2

N. diseases: 17
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.030 1.000 3 2010 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.030 1.000 3 2010 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.030 1.000 3 1997 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.030 1.000 3 1997 2014
Male infertility
CUI: C0021364
Disease: Male infertility
137 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.020 1.000 2 2014 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2014 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2011 2011
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
247 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2017 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2009 2009
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2006 2006
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2007 2007
Slow acetylator due to N-acetyltransferase enzyme variant
CUI: C1827377
Disease: Slow acetylator due to N-acetyltransferase enzyme variant
8 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2006 2006
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
197 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 0.010 1.000 1 2014 2014