Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 2
rs7638110
MRPS22
1.000 0.080 3 139185143 intron variant G/T snv 9.4E-02 2
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 5
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 7
rs1412239
LINGO2
0.925 0.120 9 28425517 intron variant C/G snv 0.26 2
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 8
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs9299
HOXB5 ; HOXB3 ; HOXB-AS3
1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 8
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4