Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs757891309
MTR
0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs80356773
GBA
0.925 0.080 1 155235002 missense variant C/T snv 3
rs9536314
KL
0.925 0.160 13 33054001 missense variant T/A;G snv 0.14 3
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs2175898 6 151875817 intron variant C/G;T snv 2
rs7208505 1.000 0.040 17 59110368 3 prime UTR variant G/A;C;T snv 2
rs1080963 22 15376497 intergenic variant C/T snv 1
rs138191010 7 145416641 intergenic variant G/T snv 1
rs1403522266 4 47320137 missense variant A/G snv 4.0E-06 1
rs713224 4 186491213 intron variant G/A;C snv 1
rs749865093 11 18029360 missense variant C/T snv 3.2E-05 1
rs753009654 6 6002360 missense variant C/A;T snv 4.0E-06 1
rs757522886
MTR
1 236885125 missense variant C/T snv 8.0E-06 1
rs8836 17 76081416 3 prime UTR variant G/A;C;T snv 1.6E-05; 0.54; 4.8E-05 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1290141855 1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1200746244 0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs368939818 0.763 0.280 11 49156734 missense variant G/A snv 4.0E-05 2.1E-05 13
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs387906315
GBA
0.790 0.160 1 155240660 frameshift variant -/C delins 5.2E-05 5.6E-05 8
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs115482041 0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs2228305 0.925 0.120 17 82084916 missense variant C/T snv 4.1E-02 4.5E-02 3
rs12720208 0.925 0.040 8 16992890 3 prime UTR variant G/A snv 5.5E-02 3