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: rs11119805
rs11119805
1 211744902 3 prime UTR variant T/A snv 0.13
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs11120822
rs11120822
1 7053052 intron variant G/C snv 0.34
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs1514178
rs1514178
1 60739797 intron variant T/C snv 1.5E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2391388
rs2391388
1 95020269 intron variant A/C snv 0.49
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs3845427
rs3845427
1 181293302 intergenic variant T/A snv 0.52
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs6671200
rs6671200
1 95231973 intron variant A/C snv 0.90
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs6675668
rs6675668
1 95050081 intron variant T/G snv 0.43
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs860873
rs860873
1 94921652 intron variant G/A snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs9437689
rs9437689
1 95083980 regulatory region variant C/T snv 0.34
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 2 2011 2013
dbSNP: rs12472274
rs12472274
2 238186781 non coding transcript exon variant G/A;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs1260326
rs1260326
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1260333
rs1260333
0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1424760
rs1424760
2 162925277 intergenic variant C/T snv 0.52
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs16832011
rs16832011
LCT
2 135787729 downstream gene variant A/G snv 5.1E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2118674
rs2118674
2 170462384 intron variant A/T snv 0.87
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs2911711
rs2911711
0.925 0.120 2 27527679 downstream gene variant T/A snv 0.58
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs4666002
rs4666002
0.925 0.120 2 27617773 intron variant G/A;C snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs6722456
rs6722456
2 133771520 intergenic variant G/A snv 4.5E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs197770
rs197770
3 37474336 intron variant A/G snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs334809
rs334809
0.925 0.080 3 3088537 intron variant A/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs9832727
rs9832727
3 142930268 intron variant C/A;G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs11730235
rs11730235
4 26922822 intron variant G/T snv 0.26
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs6844153
rs6844153
4 26942692 intron variant C/T snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011