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
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
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
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
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
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
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
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 4
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 4
rs1490384 6 126530014 intron variant C/G;T snv 4
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 4
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs1254337
C14orf39
0.925 0.120 14 60453807 intron variant A/T snv 0.37 3
rs16917237
BDNF ; BDNF-AS
11 27680836 intron variant G/T snv 0.16 3
rs246185
MIR193BHG
16 14301575 intron variant T/C snv 0.34 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3