Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs879254728
LDLR
0.882 0.080 19 11107511 missense variant T/C;G snv 3
rs879254725
LDLR
0.925 0.080 19 11107508 stop gained G/T snv 2
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs846906
HSD11B1 ; HSD11B1-AS1
1.000 0.040 1 209714373 intron variant T/A;C snv 1
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 3
rs8177409
GPX3 ; LOC105378228
1.000 0.040 5 151020289 upstream gene variant A/T snv 0.15 1
rs8122
STEAP4
1.000 0.040 7 88276856 3 prime UTR variant T/A;C snv 1
rs8066560
SREBF1
0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs8064821
SOCS3 ; LOC101928674
0.851 0.120 17 78361310 intron variant C/A snv 0.17 6
rs806379
CNR1
1.000 0.040 6 88151548 intron variant A/C;T snv 2
rs8060686
EDC4
1.000 0.040 16 67877614 synonymous variant T/C snv 0.23 0.32 2
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 5
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs7965413
VWF
1.000 0.040 12 6125723 upstream gene variant C/T snv 0.53 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7865146 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 2
rs7849191
JAK2
0.882 0.120 9 4988761 intron variant C/T snv 0.50 3
rs7841189 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 3