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
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 3
rs9817981
TP63
1.000 0.040 3 189845741 intron variant A/G;T snv 1
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs887304
CRACR2A
0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs822393
ADIPOQ
0.882 0.160 3 186848537 intron variant C/T snv 0.30 3
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8187710
ABCC2
0.827 0.200 10 99851537 missense variant G/A snv 5.3E-02 8.5E-02 6
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7946
PEMT
0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 6
rs781469754
MTTP
1.000 0.040 4 99591691 missense variant A/G snv 4.0E-06 7.0E-06 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs768007422
ARHGEF7
1.000 0.040 13 111277667 missense variant C/G snv 1
rs7674434
KLB
0.925 0.120 4 39417789 intron variant T/G snv 0.32 2
rs7649970
PPARG
1.000 0.040 3 12350773 intron variant C/T snv 0.14 2
rs762049291
CCR2
1.000 0.040 3 46358410 missense variant A/G;T snv 4.0E-06; 4.0E-06 1
rs756998920
MTTP
1.000 0.040 4 99581967 missense variant G/A snv 3.4E-04 8.4E-05 1
rs753885266
SLC17A5
1.000 0.040 6 73621899 missense variant C/T snv 4.0E-06 7.0E-06 1
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3