Source: GWASCAT

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: rs2244608
rs2244608
0.882 0.160 12 120979185 intron variant A/G snv 0.29
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.700 1.000 1 2019 2019
dbSNP: rs1169288
rs1169288
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
0.700 1.000 1 2018 2018
dbSNP: rs80019595
rs80019595
12 120979503 intron variant C/G;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.700 1.000 1 2019 2019
dbSNP: rs1169286
rs1169286
1.000 0.080 12 120981253 intron variant T/C snv 0.39
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
0.700 1.000 1 2018 2018
dbSNP: rs1183910
rs1183910
1.000 0.080 12 120983004 intron variant G/A snv 0.28
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 5 2009 2019
dbSNP: rs7310409
rs7310409
0.925 0.160 12 120987058 intron variant A/C;G;T snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 4 2008 2019
dbSNP: rs2393791
rs2393791
0.925 0.160 12 120986153 intron variant C/T snv 0.62
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 3 2013 2019
dbSNP: rs1169310
rs1169310
12 121001630 3 prime UTR variant G/A snv 0.31
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2008 2019
dbSNP: rs2259816
rs2259816
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2012 2019
dbSNP: rs7979473
rs7979473
12 120982457 intron variant A/C;G snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2012 2019
dbSNP: rs1169284
rs1169284
12 120982123 intron variant T/C snv 0.32
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs9738226
rs9738226
12 120985856 intron variant A/G snv 0.62
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2255531
rs2255531
12 120977112 intron variant G/A snv 0.35
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1169288
rs1169288
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35
CUI: C0201952
Disease: Chloride measurement
Chloride measurement
0.700 1.000 1 2018 2018
dbSNP: rs2244608
rs2244608
0.882 0.160 12 120979185 intron variant A/G snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 3 2017 2018
dbSNP: rs1169288
rs1169288
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 2 2009 2018
dbSNP: rs2259816
rs2259816
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2009 2011
dbSNP: rs1169288
rs1169288
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35
Diabetes Mellitus, Non-Insulin-Dependent
0.780 1.000 1 2006 2018
dbSNP: rs1169299
rs1169299
1.000 0.080 12 120991391 intron variant T/C snv 0.43
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs12427353
rs12427353
1.000 0.080 12 120989098 intron variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.800 1.000 1 2012 2012
dbSNP: rs1800574
rs1800574
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.850 0.857 1 2004 2018
dbSNP: rs1169299
rs1169299
1.000 0.080 12 120991391 intron variant T/C snv 0.43
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs766982432
rs766982432
12 120994315 frameshift variant C/-;CC;CCC delins
CUI: C0017979
Disease: Glycosuria
Glycosuria
0.700 1.000 1 2019 2019
dbSNP: rs780518365
rs780518365
12 120992362 intron variant A/G snv
CUI: C0017979
Disease: Glycosuria
Glycosuria
0.700 1.000 1 2019 2019
dbSNP: rs2244608
rs2244608
0.882 0.160 12 120979185 intron variant A/G snv 0.29
High density lipoprotein measurement
0.700 1.000 1 2019 2019