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
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
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
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
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 5
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
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
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
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7