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
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 2
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 3
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 1
rs3746619
MC3R
0.925 0.200 20 56248749 5 prime UTR variant C/A snv 0.14 0.21 1
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 1
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs2194899
RXRG
1.000 0.160 1 165441548 intron variant A/G snv 0.51 1
rs4889
KISS1
0.882 0.160 1 204190659 missense variant G/A;C snv 5.2E-06; 0.29 1
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
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
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 4
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 2
rs1254337
C14orf39
0.925 0.120 14 60453807 intron variant A/T snv 0.37 1
rs2798224
MSANTD1
1.000 0.120 4 3265941 intron variant G/A snv 0.45 1
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 1
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7