Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17150703 1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02 2
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 5
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 9
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 7
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs4735692 1.000 0.080 8 75703428 intergenic variant A/G snv 0.48 2
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 2
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs6711012 1.000 0.080 2 624034 intergenic variant G/A;C;T snv 2
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 5