Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 3
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 3
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 2
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 2
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 2
rs13447324
MC4R
1.000 0.080 18 60372245 stop gained G/T snv 6.8E-05 1.3E-04 2
rs1412239
LINGO2
0.925 0.120 9 28425517 intron variant C/G snv 0.26 2
rs1514174
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74527379 intron variant C/T snv 0.44 2
rs1514177
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.080 1 74525718 intron variant C/G snv 0.49 2
rs17150703 1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02 2
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
rs6711012 1.000 0.080 2 624034 intergenic variant G/A;C;T snv 2
rs7638110
MRPS22
1.000 0.080 3 139185143 intron variant G/T snv 9.4E-02 2
rs9299
HOXB5 ; HOXB3 ; HOXB-AS3
1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv 2
rs9568867 1.000 0.080 13 53533217 intron variant G/A snv 0.13 2