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: rs4846914
rs4846914
0.925 0.080 1 230159944 intron variant G/A snv 0.45
High density lipoprotein measurement
0.800 1.000 5 2008 2019
dbSNP: rs4846914
rs4846914
0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2008 2019
dbSNP: rs2144300
rs2144300
0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2018
dbSNP: rs2144300
rs2144300
0.882 0.040 1 230159169 intron variant C/T snv 0.44
High density lipoprotein measurement
0.800 1.000 2 2008 2018
dbSNP: rs10489615
rs10489615
1 230169242 intron variant A/C;G snv
High density lipoprotein measurement
0.800 1.000 1 2010 2010
dbSNP: rs4846922
rs4846922
1.000 0.040 1 230171436 intron variant T/A;C;G snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2012 2012
dbSNP: rs2144300
rs2144300
0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2011 2013
dbSNP: rs4846914
rs4846914
0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 5 2008 2013
dbSNP: rs2144300
rs2144300
0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2008 2012
dbSNP: rs4846918
rs4846918
1 230164840 intron variant C/G;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs4846918
rs4846918
1 230164840 intron variant C/G;T snv
High density lipoprotein measurement
0.700 1.000 2 2012 2012
dbSNP: rs10489615
rs10489615
1 230169242 intron variant A/C;G snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2010 2010
dbSNP: rs17315646
rs17315646
1 230159560 intron variant C/A;G snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs17315646
rs17315646
1 230159560 intron variant C/A;G snv 0.45
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs17315646
rs17315646
1 230159560 intron variant C/A;G snv 0.45
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2281719
rs2281719
1.000 0.040 1 230161913 intron variant C/T snv 0.45
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2281719
rs2281719
1.000 0.040 1 230161913 intron variant C/T snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2281719
rs2281719
1.000 0.040 1 230161913 intron variant C/T snv 0.45
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2296065
rs2296065
1 230166030 intron variant G/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2296065
rs2296065
1 230166030 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2296065
rs2296065
1 230166030 intron variant G/A;C snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs4846908
rs4846908
1 230149309 intron variant G/A snv 0.43
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs4846908
rs4846908
1 230149309 intron variant G/A snv 0.43
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs4846914
rs4846914
0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs4846918
rs4846918
1 230164840 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012