Source: GWASDB

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: rs10195252
rs10195252
0.925 0.080 2 164656581 intron variant T/C snv 0.48
Diabetes Mellitus, Non-Insulin-Dependent
0.810 1.000 1 2012 2019
dbSNP: rs12328675
rs12328675
2 164684290 3 prime UTR variant T/C snv 0.13
High density lipoprotein measurement
0.800 1.000 2 2010 2019
dbSNP: rs10195252
rs10195252
0.925 0.080 2 164656581 intron variant T/C snv 0.48
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2010 2010
dbSNP: rs10195252
rs10195252
0.925 0.080 2 164656581 intron variant T/C snv 0.48
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.800 1.000 1 2010 2019
dbSNP: rs13389219
rs13389219
1.000 0.080 2 164672366 intron variant C/T snv 0.47
Diabetes Mellitus, Non-Insulin-Dependent
0.800 1.000 1 2012 2018
dbSNP: rs13389219
rs13389219
1.000 0.080 2 164672366 intron variant C/T snv 0.47
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.800 1.000 1 2013 2019
dbSNP: rs12328675
rs12328675
2 164684290 3 prime UTR variant T/C snv 0.13
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
dbSNP: rs1128249
rs1128249
1.000 0.080 2 164672114 intron variant G/C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2012 2012
dbSNP: rs13389219
rs13389219
1.000 0.080 2 164672366 intron variant C/T snv 0.47
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs13389219
rs13389219
1.000 0.080 2 164672366 intron variant C/T snv 0.47
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs13389219
rs13389219
1.000 0.080 2 164672366 intron variant C/T snv 0.47
High density lipoprotein measurement
0.700 1.000 1 2012 2012