Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 2
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 5
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 2
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 3
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs1514177
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.080 1 74525718 intron variant C/G snv 0.49 2
rs4735692 1.000 0.080 8 75703428 intergenic variant A/G snv 0.48 2
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs1514174
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74527379 intron variant C/T snv 0.44 2
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 9
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 3
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 8
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 6
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16