Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9906827
RPTOR
0.925 0.120 17 80691605 intron variant C/A;T snv 2
rs953686324
CLCNKB
0.851 0.160 1 16044506 frameshift variant -/G delins 4.3E-06 5.6E-05 7
rs8066560
SREBF1
0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs80356618
KCNJ11
0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs80356616
KCNJ11
0.732 0.360 11 17387917 missense variant C/T snv 19
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs776793516
HNF1A
0.925 0.080 12 120997492 frameshift variant CA/- delins 4.0E-06 2
rs775776658
ABCC8
1.000 0.040 11 17474926 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.0E-05 1
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs764437500
EHMT1
0.925 0.080 9 137716697 missense variant G/A snv 4.0E-06 2
rs764232985
GCK
0.851 0.080 7 44153381 missense variant C/G;T snv 4.0E-06 4
rs755498926
GCK
1.000 0.040 7 44145228 missense variant T/C snv 4.1E-06 1
rs751279776
LOC105375258 ; GCK
0.925 0.080 7 44149986 missense variant C/T snv 4.0E-06 2
rs750931344
SLC38A4
1.000 0.040 12 46769424 missense variant C/T snv 4.0E-06 1
rs746913146
LOC105375258 ; GCK
1.000 0.040 7 44149816 missense variant G/A snv 4.0E-06 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6084264
AVP
1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 1
rs59852838
ABCC8
0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 3