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
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 7
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 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
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 5
rs900145 11 13272358 upstream gene variant C/T snv 0.62 4
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 4