Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 3
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs1555543 1 96479241 intergenic variant A/C snv 0.55 2
rs261967
LOC101929710 ; LOC107986362
5 96514546 intron variant A/C snv 0.42 2
rs3736594
MRPL33
2 27772914 intron variant A/C snv 0.62 2
rs2390669
STK39
1.000 0.040 2 168235432 intron variant A/C snv 0.14 1
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 1
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5