Disease: Finding of body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10077823
LOC101929710 ; LOC107986362
5 96510626 intron variant A/G snv 0.43 2
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15 3
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 4
rs1026534
LOC101929710 ; LOC107986362
5 96519387 intron variant G/C snv 0.60 2
rs10476682
LOC101929710
5 96522554 intron variant A/G snv 0.38 2
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 4
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 3
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs11231111
AHNAK
11 62492533 intron variant C/T snv 0.15 2
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 4
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74534327 intron variant -/T delins 2
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 5
rs1167800
HIP1
7 75546898 intron variant A/G snv 0.34 3
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs1211166
NTRK2
9 84671077 intron variant G/A snv 0.77 2
rs12142020
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1 74534327 intron variant A/T snv 0.50 2
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 8