Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs75766425
NID2
14 52045193 intron variant G/C snv 3.0E-03 2
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs730180
BBS4
15 72715552 intron variant G/A snv 0.72 2
rs8027181
ADPGK-AS1
15 72796528 intron variant A/T snv 0.57 2
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16