Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908672
LRP5
0.925 0.080 11 68357802 missense variant C/T snv 3
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs942758928
MC4R
1.000 0.080 18 60371854 missense variant C/T snv 8.0E-06 1.4E-05 2
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 14
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs28934897
MVK
0.790 0.400 12 109596515 missense variant G/A snv 1.6E-03 1.5E-03 10
rs104895321
MVK
0.882 0.240 12 109591301 missense variant C/G;T snv 1.4E-04 4
rs104895358
MVK
12 109595148 missense variant G/A snv 1.2E-05 2
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs148881970
NAGLU
0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs555145190
NAGLU
0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs121908153
NLRP3
0.882 0.080 1 247424356 missense variant G/A;C snv 4
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs6191
NR3C1
0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs778899140
PDE10A
0.925 6 165450268 missense variant T/C snv 4.0E-06 5
rs875989839
PDE10A
1.000 6 165450242 missense variant C/G snv 3
rs397515323
PDK3
0.851 0.080 X 24503479 missense variant G/A snv 7