Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11039149
rs11039149
0.827 0.280 11 47255124 intron variant A/G snv 0.19
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs11039149
rs11039149
0.827 0.280 11 47255124 intron variant A/G snv 0.19
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs11039149
rs11039149
0.827 0.280 11 47255124 intron variant A/G snv 0.19
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs12221497
rs12221497
0.882 0.160 11 47259102 splice region variant G/A snv 0.11
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2279238
rs2279238
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3758673
rs3758673
0.925 0.120 11 47257366 intron variant C/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2009 2012
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
High density lipoprotein measurement
0.800 1.000 2 2009 2012
dbSNP: rs10838681
rs10838681
1.000 0.040 11 47253513 intron variant G/A snv 0.34
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.800 1.000 1 2012 2012
dbSNP: rs2279238
rs2279238
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs2279238
rs2279238
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2279238
rs2279238
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11039155
rs11039155
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.020 1.000 2 2008 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.020 1.000 2 2012 2013
dbSNP: rs2279238
rs2279238
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
Stage IIA Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C4525305
Disease: Stage IV Gallbladder Cancer AJCC v8
Stage IV Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
Stage 0 Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
Stage IIB Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2013 2013
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
Stage III Gallbladder Cancer AJCC v8
0.010 < 0.001 1 2013 2013
dbSNP: rs11039155
rs11039155
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 0.500 2 2012 2014
dbSNP: rs1449626
rs1449626
1.000 0.040 11 47269208 5 prime UTR variant A/C snv 0.26
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 1.000 1 2014 2014
dbSNP: rs1449627
rs1449627
1.000 0.040 11 47269433 5 prime UTR variant T/C;G snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 1.000 1 2014 2014