Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
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
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
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
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
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs75766425
NID2
14 52045193 intron variant G/C snv 3.0E-03 2
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16