Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 8
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 7
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6