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: rs17606561
rs17606561
1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 2 2011 2012
dbSNP: rs10498676
rs10498676
0.925 0.040 6 11026766 intron variant G/A snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs12195587
rs12195587
6 10989709 synonymous variant G/A snv 0.12 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1225737
rs1225737
6 10982419 3 prime UTR variant C/T snv 0.59
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1321536
rs1321536
6 11018579 intron variant T/A;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1323739
rs1323739
6 11004328 intron variant C/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs1570069
rs1570069
6 11017592 intron variant A/G snv 0.54
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17675073
rs17675073
6 11008416 intron variant G/A snv 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17764592
rs17764592
6 11002911 intron variant A/C;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2180725
rs2180725
6 11025187 intron variant T/C snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2236212
rs2236212
1.000 0.040 6 10994782 intron variant G/C snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2281591
rs2281591
6 10990260 intron variant A/G snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2295601
rs2295601
6 11005453 synonymous variant G/A snv 0.22 0.21
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2295602
rs2295602
6 11005609 intron variant T/C snv 0.57 0.54
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3734398
rs3734398
6 10982740 3 prime UTR variant T/C snv 0.41
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3756963
rs3756963
0.882 0.200 6 11021921 intron variant T/C snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3778166
rs3778166
6 11032931 intron variant G/A snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798707
rs3798707
6 10991702 intron variant C/T snv 0.53
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798709
rs3798709
6 11001043 intron variant A/G snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798710
rs3798710
6 11002550 intron variant G/C snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798711
rs3798711
6 11002577 intron variant T/C snv 0.52
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798713
rs3798713
6 11008389 intron variant G/C snv 0.41
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798719
rs3798719
6 11036592 intron variant C/T snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798721
rs3798721
6 11039950 intron variant A/C snv 0.31
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs3798722
rs3798722
6 11040190 intron variant A/G snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011