Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 3
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs12221497
NR1H3
0.882 0.160 11 47259102 splice region variant G/A snv 0.11 4
rs4641
LMNA
0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs745975
HNF4A
0.925 0.080 20 44406053 splice region variant C/T snv 0.20 0.18 2
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 7