Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs80338903
USH2A
0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs387906315
GBA
0.790 0.160 1 155240660 frameshift variant -/C delins 5.2E-05 5.6E-05 8
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs1558027212
TMCO1
0.827 0.320 1 165728096 frameshift variant GC/- del 7
rs3219484
MUTYH
0.807 0.160 1 45334484 missense variant C/A;T snv 4.8E-02 4.8E-02 7
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs80356733
TARDBP
0.790 0.200 1 11022451 missense variant G/T snv 7
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs863225264
MTOR
0.827 0.240 1 11130747 missense variant C/T snv 6
rs112422930
MUTYH
0.882 0.160 1 45332409 missense variant A/C snv 7.0E-06 4