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
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
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
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs1059004
OLIG2
0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs10812227
VLDLR-AS1
1.000 0.080 9 2548556 intron variant C/G;T snv 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1106076 1.000 0.080 7 5581212 regulatory region variant C/A;G snv 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
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
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
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
rs121918805
LOC102724058 ; SCN1A-AS1 ; SCN1A
0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6