Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 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
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs730180
BBS4
15 72715552 intron variant G/A snv 0.72 2
rs75766425
NID2
14 52045193 intron variant G/C snv 3.0E-03 2
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs8027181
ADPGK-AS1
15 72796528 intron variant A/T snv 0.57 2