Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1412239
LINGO2
0.925 0.120 9 28425517 intron variant C/G snv 0.26 2
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
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
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 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
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 8
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 8
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
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
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
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs13447324
MC4R
1.000 0.080 18 60372245 stop gained G/T snv 6.8E-05 1.3E-04 2