Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 3
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs4549631 6 126645162 intron variant T/C;G snv 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs7846385 8 77247943 intergenic variant T/C snv 0.23 2
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 2
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 2
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 2
rs7861820
LINC01505
9 106174393 intron variant T/C snv 0.62 2
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 2
rs12374521
LOC107986462 ; HTR4
5 148457317 intron variant C/T snv 0.45 2
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 2
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 1
rs10940138 5 67898641 intron variant C/T snv 0.21 1