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: rs4660293
rs4660293
1 39562508 non coding transcript exon variant A/C;G snv
High density lipoprotein measurement
0.800 1.000 5 2010 2018
dbSNP: rs3768321
rs3768321
1.000 0.080 1 39570256 intron variant G/T snv 0.14
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 2 2016 2018
dbSNP: rs3768321
rs3768321
1.000 0.080 1 39570256 intron variant G/T snv 0.14
RDW - Red blood cell distribution width result
0.700 1.000 2 2016 2019
dbSNP: rs3768321
rs3768321
1.000 0.080 1 39570256 intron variant G/T snv 0.14
Red cell distribution width determination
0.700 1.000 2 2016 2019
dbSNP: rs17513135
rs17513135
1.000 0.080 1 39570014 intron variant C/A;T snv 0.17 0.16
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs17513135
rs17513135
1.000 0.080 1 39570014 intron variant C/A;T snv 0.17 0.16
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2019 2019
dbSNP: rs2293476
rs2293476
1 39571175 3 prime UTR variant G/C snv 0.16
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs3768321
rs3768321
1.000 0.080 1 39570256 intron variant G/T snv 0.14
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs3768321
rs3768321
1.000 0.080 1 39570256 intron variant G/T snv 0.14
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs41264487
rs41264487
1 39571682 synonymous variant C/G;T snv 0.13; 4.9E-05
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2018 2018
dbSNP: rs4660293
rs4660293
1 39562508 non coding transcript exon variant A/C;G snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs4660293
rs4660293
1 39562508 non coding transcript exon variant A/C;G snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2016 2016
dbSNP: rs4660293
rs4660293
1 39562508 non coding transcript exon variant A/C;G snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs61743745
rs61743745
1 39571272 synonymous variant G/A;T snv 2.0E-02; 8.0E-06
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019