Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 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
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
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 7
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
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
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 2
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs6711012 1.000 0.080 2 624034 intergenic variant G/A;C;T snv 2
rs6752378 1.000 0.080 2 24927247 intergenic variant C/A snv 0.57 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 4
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs7638110
MRPS22
1.000 0.080 3 139185143 intron variant G/T snv 9.4E-02 2
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 2