Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 4
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 4
rs11161721
COL24A1
1 86022231 intron variant C/A snv 0.27 0.27 4
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 4
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 3
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 3
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 3
rs9552416 13 18737101 downstream gene variant C/A;T snv 3
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 3
rs2300835
AKAP6
14 32738316 intron variant C/A snv 0.16 3
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 3