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: rs34574998
rs34574998
12 57154581 synonymous variant T/C snv 2.3E-02 4.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs34614287
rs34614287
12 57155352 3 prime UTR variant C/G snv 6.8E-04
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs34630693
rs34630693
12 57212472 missense variant C/A;T snv 1.2E-05; 2.0E-05
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs35161844
rs35161844
12 57184057 intron variant C/T snv 7.2E-03 2.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs35253246
rs35253246
12 57155077 3 prime UTR variant T/G snv 5.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs35599705
rs35599705
12 57175044 intron variant G/A snv 1.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012