Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010553
STAB1
1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 2
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12500837
NMU
1.000 0.080 4 55627872 intron variant T/C snv 0.21 1
rs1256046734
LEPR
0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1319501
NAMPT
0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 4
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs149106723
NMU
1.000 0.080 4 55599178 missense variant G/A snv 1.6E-05 4.2E-05 1
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs162430
PYY
1.000 0.080 17 43953041 3 prime UTR variant G/A snv 0.23 1
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs1800849
UCP3
0.851 0.160 11 74009120 upstream gene variant G/A;T snv 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1996023 0.925 0.120 4 45162620 intergenic variant T/A;G snv 3
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv 3
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 7
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs2285053
MMP2
0.752 0.320 16 55478465 intron variant C/T snv 0.12 15