Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 7
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
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
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 4
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 4
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs1412239
LINGO2
0.925 0.120 9 28425517 intron variant C/G snv 0.26 2
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
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
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14