Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10077823
LOC101929710 ; LOC107986362
5 96510626 intron variant A/G snv 0.43 2
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15 2
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3
rs10173167 2 646767 intergenic variant G/A snv 0.82 2
rs10188334 2 653874 regulatory region variant C/A;T snv 0.15 2
rs10193244 2 647580 intergenic variant T/C snv 0.77 2
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs1026534
LOC101929710 ; LOC107986362
5 96519387 intron variant G/C snv 0.60 2
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs10476682
LOC101929710
5 96522554 intron variant A/G snv 0.38 2
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 2
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 3
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 4
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3
rs10993160 9 94306644 downstream gene variant A/G snv 4.2E-02 2
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 2
rs1106683 7 131768766 intergenic variant G/A snv 0.14 2
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4