Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs4662344
ARHGAP15
0.925 0.080 2 143591289 intron variant T/C snv 0.82 3
rs962369
BDNF
11 27712873 intron variant T/C snv 0.24 3
rs7609897
COLQ
0.925 0.080 3 15461174 intron variant G/T snv 0.22 3
rs67153654
FAM155A
0.925 0.080 13 107572636 intron variant T/A;C snv 3
rs61823192
LYPLAL1-DT
1 219121228 intron variant C/T snv 1.6E-02 3
rs582094
ABO
9 133270074 intron variant T/A snv 2
rs2028386
LOXL1
1.000 0.040 15 73934367 intron variant C/A;G snv 2
rs10472291 5 37772678 regulatory region variant C/A snv 0.42 1
rs115490395 1 110120397 intergenic variant T/A snv 7.8E-03 1
rs139711468 12 19939051 intron variant G/A snv 1.5E-02 1
rs189921337 7 67679580 intergenic variant C/T snv 3.3E-03 1
rs200217504 4 162280954 intergenic variant -/A;G;T ins 1
rs2470653 3 5804815 intergenic variant T/A;C snv 1
rs2784255 1 220893031 intergenic variant T/C snv 0.56 1
rs428022 15 67956797 intergenic variant A/G;T snv 1
rs4461115 17 47722212 regulatory region variant T/C snv 0.19 1
rs4839715 6 97917413 intron variant G/A snv 0.27 1
rs4871180 8 121246834 regulatory region variant C/T snv 0.26 1
rs73230688 7 96880690 intergenic variant C/T snv 0.36 1
rs74159124 10 122365153 intergenic variant T/C snv 5.3E-02 1
rs759555 18 57223332 regulatory region variant T/C snv 0.72 1
rs7608769 2 158740458 intron variant A/C;T snv 1
rs79586998 18 70617285 intergenic variant C/T snv 1.9E-02 1
rs8074740 17 44235410 regulatory region variant G/A snv 0.41 1