Source: GWASDB

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: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs174585
rs174585
11 61844222 intron variant G/A;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174589
rs174589
11 61848331 intron variant C/G;T snv 0.19
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174591
rs174591
11 61850204 intron variant T/A;G snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174593
rs174593
11 61851359 intron variant T/C snv 0.24
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174597
rs174597
11 61853568 intron variant G/A;C;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174601
rs174601
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
0.800 1.000 1 2011 2011
dbSNP: rs174602
rs174602
1.000 0.080 11 61856942 non coding transcript exon variant T/C snv 0.37
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174605
rs174605
11 61859449 intron variant G/T snv 0.20
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174611
rs174611
11 61860409 intron variant T/C snv 0.21
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174616
rs174616
1.000 0.080 11 61861650 intron variant G/A snv 0.51
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17764324
rs17764324
11 61867616 downstream gene variant G/A;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17831757
rs17831757
11 61867728 downstream gene variant T/C snv 9.3E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2072114
rs2072114
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2524299
rs2524299
11 61837310 intron variant A/T snv 0.17
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2526678
rs2526678
11 61856321 non coding transcript exon variant G/A snv 8.6E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2727270
rs2727270
11 61835765 intron variant C/T snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2727271
rs2727271
11 61835886 intron variant A/T snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2845573
rs2845573
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2851682
rs2851682
11 61848540 intron variant A/G snv 9.9E-02
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: rs4246215
rs4246215
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs498793
rs498793
1.000 0.040 11 61857233 intron variant T/C snv 0.62
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs526126
rs526126
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011