Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2289277
TSLP
1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv 3
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs2605100
LOC107985272 ; LYPLAL1-AS1
1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 3
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs26802
GHRLOS ; GHRL
0.925 0.160 3 10290681 intron variant T/G snv 0.31 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03 5
rs35036378
ESR2
0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 5
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs562962093
MBL2
0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs6219
HELLPAR ; LINC02456 ; IGF1
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02 2
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33