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: rs7190458
rs7190458
1.000 0.120 16 75229763 synonymous variant G/A snv 5.1E-02 0.11
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 2 2014 2018
dbSNP: rs1035539
rs1035539
1.000 0.080 16 75242877 missense variant G/A;C snv 0.68; 4.1E-06
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic
Digestive System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11649684
rs11649684
1.000 0.080 16 75269081 upstream gene variant G/A snv 0.71
CUI: C0376670
Disease: Pancreatitis, Alcoholic
Pancreatitis, Alcoholic
Digestive System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2018 2018
dbSNP: rs16957552
rs16957552
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16957552
rs16957552
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs16957552
rs16957552
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16957552
rs16957552
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4888362
rs4888362
16 75234347 intron variant T/C snv 0.80
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs774390402
rs774390402
16 75235116 missense variant A/C snv 1.2E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2008 2008