Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2289277
TSLP
1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv 3
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 5
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs3748024
CHCHD5
0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs750359414
RETN
0.851 0.240 19 7669884 missense variant C/G;T snv 4.0E-06; 4.0E-06 5
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10