Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs730180
BBS4
15 72715552 intron variant G/A snv 0.72 2
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs75766425
NID2
14 52045193 intron variant G/C snv 3.0E-03 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6