Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs8027181
ADPGK-AS1
15 72796528 intron variant A/T snv 0.57 2
rs730180
BBS4
15 72715552 intron variant G/A snv 0.72 2
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs75766425
NID2
14 52045193 intron variant G/C snv 3.0E-03 2
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6