Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs1564421528
WAC
0.882 0.080 10 28614666 stop gained C/T snv 16
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs1057524157
DEAF1
0.776 0.200 11 686962 missense variant A/C;T snv 19
rs1554944271
DEAF1
0.851 0.240 11 686925 missense variant C/G snv 14
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs3789327
ARNTL
0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs11600996
ARNTL
1.000 0.040 11 13374619 intron variant T/C snv 0.40 4
rs1982350
ARNTL
11 13328584 intron variant A/G snv 0.57 4
rs1481892
ARNTL
11 13280374 intron variant G/C snv 0.62 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1057524820
SCN8A
0.776 0.280 12 51765746 missense variant G/A;T snv 33
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs281864996
GNPTAB
0.807 0.280 12 101764363 frameshift variant CTTTT/-;CTTTTCTTTT delins 2.8E-05 7.0E-06 10
rs2291739
TIMELESS
0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs397507562
GNPTAB
0.851 0.240 12 101757311 splice acceptor variant C/G;T snv 6
rs1229030855
TIMELESS
0.925 0.080 12 56428321 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs75184679
RNASEH2B
0.776 0.360 13 50945445 missense variant G/A snv 1.4E-03 1.4E-03 16
rs9315202 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 4