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: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 9 2007 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.800 1.000 6 2010 2019
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2011 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2011 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 3 2017 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 3 2012 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.830 1.000 3 2010 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
Diabetes Mellitus, Non-Insulin-Dependent
0.900 1.000 3 2007 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
Low density lipoprotein cholesterol measurement
0.800 1.000 3 2008 2019
dbSNP: rs3817588
rs3817588
0.882 0.160 2 27508345 intron variant T/C snv 0.14
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.800 1.000 2 2009 2015
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.800 1.000 2 2011 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2008 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.800 1.000 2 2011 2018
dbSNP: rs3817588
rs3817588
0.882 0.160 2 27508345 intron variant T/C snv 0.14
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2016 2016
dbSNP: rs3817588
rs3817588
0.882 0.160 2 27508345 intron variant T/C snv 0.14
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2016 2016
dbSNP: rs57634090
rs57634090
2 27508873 intron variant T/-;TT;TTT;TTTT;TTTTTT delins
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2019 2019
dbSNP: rs6547692
rs6547692
1.000 0.080 2 27512105 intron variant G/A snv 0.58
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs6547692
rs6547692
1.000 0.080 2 27512105 intron variant G/A snv 0.58
CUI: C0201952
Disease: Chloride measurement
Chloride measurement
0.700 1.000 1 2018 2018
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2017
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.800 1.000 1 2011 2012