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: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 3 2011 2013
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.800 2 2012 2013
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
High density lipoprotein measurement
0.800 1 2010 2012
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1 2010 2010
dbSNP: rs174538
rs174538
0.821 0.143 11 61792609 5 prime UTR variant G/A snp 0.34 0.27
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 2 2012 2013
dbSNP: rs102274
rs102274
11 61790354 non coding transcript exon variant T/C snp 0.30
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2012 2012
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
Low density lipoprotein cholesterol measurement
0.700 1 2012 2012
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1 2010 2010
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1 2012 2012
dbSNP: rs102275
rs102275
0.878 0.179 11 61790331 non coding transcript exon variant T/C snp 0.47
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1 2012 2012
dbSNP: rs174538
rs174538
0.821 0.143 11 61792609 5 prime UTR variant G/A snp 0.34 0.27
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1 2011 2011
dbSNP: rs412334
rs412334
11 61792789 5 prime UTR variant C/T snp 9.8E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1 2011 2011
dbSNP: rs412334
rs412334
11 61792789 5 prime UTR variant C/T snp 9.8E-02
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2012 2012
dbSNP: rs695867
rs695867
11 61793816 intron variant A/G snp 2.4E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1 2011 2011
dbSNP: rs7102974
rs7102974
11 61792563 5 prime UTR variant C/T snp 8.5E-03 7.7E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1 2011 2011
dbSNP: rs740006
rs740006
11 61790396 3 prime UTR variant T/C snp 8.9E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1 2011 2011
dbSNP: rs740006
rs740006
11 61790396 3 prime UTR variant T/C snp 8.9E-02
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1 2012 2012