Source: GWASCAT ×
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 18
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 7
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 7
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
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 4
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 3
rs1490384 6 126530014 intron variant C/G;T snv 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
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64 2
rs10980926
ZNF483
9 111531354 intron variant A/G snv 0.56 2
rs11209943
LOC105378797
1 72284817 intron variant A/G snv 0.53 2
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 2
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 2
rs12462111
NTN5 ; SEC1P
19 48668049 intron variant C/T snv 0.33 2