Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs10261878 7 25910925 intergenic variant A/C snv 0.80 1
rs1555543 1 96479241 intergenic variant A/C snv 0.55 1
rs261967
LOC101929710 ; LOC107986362
5 96514546 intron variant A/C snv 0.42 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 1
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 2
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 3
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 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
rs9841287
LOC107986040 ; LOC105376921
3 67310 intergenic variant A/G snv 0.22 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 3
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 2
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 2