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: rs1058694
rs1058694
21 43984239 3 prime UTR variant C/T snv 0.32
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs7435
rs7435
21 43984457 3 prime UTR variant A/G snv 0.35
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs9983044
rs9983044
21 35044035 intron variant C/G snv 5.9E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs742614
rs742614
20 33894826 intergenic variant A/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs10404486
rs10404486
19 52780882 non coding transcript exon variant C/T snv 0.20
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs10414689
rs10414689
19 51293045 regulatory region variant T/C snv 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs12459897
rs12459897
19 31105872 intron variant G/T snv 1.2E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs11662721
rs11662721
18 21681452 intron variant C/T snv 0.15
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs2366017
rs2366017
17 69854760 intron variant G/A snv 2.1E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs4465599
rs4465599
16 13061021 intron variant G/A snv 0.69
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs4500751
rs4500751
16 15046354 intron variant C/T snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs4985167
rs4985167
16 14989008 non coding transcript exon variant C/T snv 0.25
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs7200543
rs7200543
16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs870288
rs870288
16 5535851 intron variant A/G snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs9932186
rs9932186
16 60280752 intergenic variant G/T snv 0.14
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs1077989
rs1077989
1.000 0.080 14 67509105 intron variant A/C snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs12587311
rs12587311
14 28647489 intergenic variant T/C snv 0.53
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs8012543
rs8012543
14 28618344 upstream gene variant G/A snv 0.50
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs10220265
rs10220265
13 103397233 downstream gene variant G/A snv 0.28
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1330767
rs1330767
13 103408241 intergenic variant C/T snv 0.21
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17648246
rs17648246
13 44919746 intergenic variant A/G snv 5.0E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2013 2013
dbSNP: rs17718828
rs17718828
13 74553977 non coding transcript exon variant C/T snv 8.8E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs2210152
rs2210152
13 103409236 intergenic variant T/C snv 0.22
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2210153
rs2210153
13 103409291 intergenic variant G/A snv 0.22
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011