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: rs13966
rs13966
11 61897520 3 prime UTR variant T/C snv 0.53
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174469
rs174469
11 61899971 intron variant C/T snv 0.14
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174472
rs174472
11 61904484 intron variant A/G snv 0.41
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174478
rs174478
11 61911104 intron variant T/G snv 0.31
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174479
rs174479
11 61911282 intron variant C/G snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17764935
rs17764935
11 61897285 downstream gene variant G/A snv 4.9E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2235093
rs2235093
11 61897650 3 prime UTR variant A/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2521568
rs2521568
11 61933461 upstream gene variant G/C snv 9.5E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2521572
rs2521572
11 61944003 regulatory region variant T/G snv 0.91
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2727261
rs2727261
11 61944659 regulatory region variant T/C;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2727266
rs2727266
11 61936862 upstream gene variant A/G snv 9.8E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs666870
rs666870
11 61910007 intron variant G/A snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174476
rs174476
11 61906646 synonymous variant C/A;G;T snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011