Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104894127
TPM2
0.925 0.080 9 35685750 missense variant G/C snv 4
rs10509125
ANK3
10 60167108 intron variant C/A snv 0.56 2
rs1059004
OLIG2
0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs1060499679
GNPTAB
0.851 0.280 12 101770496 inframe deletion GTG/- delins 5
rs1060503383
SYNGAP1
0.882 0.200 6 33441318 stop gained C/T snv 14
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs112543062
GNPTAB
0.851 0.280 12 101770161 missense variant T/C;G snv 1.2E-05 6
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs120074125
SMPD1
0.882 0.160 11 6393301 missense variant T/G snv 4.0E-06 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909671
FUS
0.851 0.120 16 31191419 missense variant G/A;T snv 4.0E-06 6
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs121918805
LOC102724058 ; SCN1A-AS1 ; SCN1A
0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs121964849
TPI1
1.000 0.120 12 6869741 missense variant A/G snv 2
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs137853208
FIGNL1 ; DDC
0.925 0.080 7 50504025 missense variant G/A snv 3
rs142441643
SDHA
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04 15