Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 5
rs750359414
RETN
0.851 0.240 19 7669884 missense variant C/G;T snv 4.0E-06; 4.0E-06 5
rs805304
CLIC1 ; DDAH2
0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 5
rs939348
THRA
0.851 0.240 17 40075600 intron variant T/C;G snv 5
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs753152
RAMP2-AS1 ; RAMP2
0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs2229765
IGF1R
0.807 0.280 15 98934996 synonymous variant G/A snv 0.40 0.39 7
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs4149601
NEDD4L
0.882 0.160 18 58149559 splice region variant G/A snv 0.28 0.33 8
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs2281939
SORBS1
0.790 0.320 10 95414595 missense variant T/C snv 8.2E-02 0.13 9
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs867593888
MYH9
0.882 0.200 22 36292059 missense variant T/C snv 11
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12