Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs12124383 1.000 0.080 1 155946002 downstream gene variant G/A snv 3.7E-03 2
rs12490383
SCAP
1.000 0.080 3 47452667 intron variant T/C snv 0.14 2
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1800247
BGLAP ; PMF1-BGLAP
0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2002880
IGF1R
1.000 0.080 15 98960516 3 prime UTR variant G/A snv 3.6E-03 2
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 5
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs225015
DIO2
0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5