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: rs174538
rs174538
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs412334
rs412334
11 61792789 5 prime UTR variant C/T snv 0.10
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs695867
rs695867
11 61793816 intron variant A/G snv 2.6E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs7102974
rs7102974
11 61792563 5 prime UTR variant C/T snv 8.5E-03 9.6E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011