Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 7
rs4969168
SOCS3
0.790 0.480 17 78357712 3 prime UTR variant A/G snv 0.71 7
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 7
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs9606756
TCN2
0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 7
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs150016118
UCP3
0.882 0.120 11 74006339 missense variant A/G snv 1.7E-05 6.3E-05 6
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6