Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113313252
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 74534327 intron variant -/T delins 2
rs201167096
FPGT-TNNI3K ; LRRC53 ; TNNI3K
1 74534327 intron variant -/T delins 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs10261878 7 25910925 intergenic variant A/C snv 0.80 3
rs1555543 1 96479241 intergenic variant A/C snv 0.55 3
rs261967
LOC101929710 ; LOC107986362
5 96514546 intron variant A/C snv 0.42 3
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 4
rs13393304 2 637830 regulatory region variant A/C;G snv 2
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 7
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7