Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012176
CTNND2
5 11320426 intron variant G/T snv 0.24 1
rs10893268
OR8A1
11 124568716 intron variant C/T snv 0.40 1
rs11059336 12 127745489 regulatory region variant T/C snv 0.14 1
rs113209956 9 25211195 intergenic variant C/T snv 5.4E-02 1
rs1181732881
DLX4
17 49969496 missense variant G/A;C;T snv 1
rs11855560
RAD51
15 40732105 3 prime UTR variant T/C snv 0.49 1
rs1192553 1 17967858 intergenic variant G/A snv 0.70 1
rs1208512188
EIF4EBP1
8 38030595 missense variant A/G snv 9.2E-06 1
rs1458103 11 81336231 intron variant A/C snv 0.25 1
rs16916239
CNGB3
8 86631513 intron variant A/G snv 0.16 1
rs2451828
ADCY2
5 7448683 intron variant C/T snv 2.7E-02 1
rs342422
EDIL3
5 84175168 intron variant G/A;C snv 1
rs34516333
ZFHX3
16 73114768 intron variant G/T snv 0.17 1
rs3828942
LEP
7 128254252 intron variant G/A snv 0.37 1
rs4692589
MFAP3L
4 170014094 intron variant A/G snv 0.44 1
rs4951043
SOX13
1 204105737 intron variant C/T snv 0.51 1
rs6030245
PTPRT
20 42441919 intron variant T/C snv 0.30 1
rs6462203
SDK1
7 3636370 intron variant C/A;T snv 1
rs72711240 4 134774652 intron variant C/T snv 2.2E-02 1
rs79928194
GIGYF2
2 232784580 intron variant T/C snv 0.14 1
rs9875578 3 13752941 intergenic variant G/A;C snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249