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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
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
rs3219484
MUTYH
0.807 0.160 1 45334484 missense variant C/A;T snv 4.8E-02 4.8E-02 7
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs112422930
MUTYH
0.882 0.160 1 45332409 missense variant A/C snv 7.0E-06 4
rs564919438
MUTYH
1.000 0.040 1 45332421 missense variant G/C;T snv 8.0E-06 2
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs544706237
REG1A
0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs1427575965
C2orf42 ; TIA1
0.925 0.120 2 70212796 missense variant G/A snv 8.0E-06 3
rs796052957
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166054735 missense variant A/G snv 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs1126680
BCHE
0.851 0.160 3 165837337 synonymous variant C/T snv 5.6E-02 5.6E-02 5
rs55781031
BCHE
0.925 0.080 3 165786432 intron variant A/G snv 5.3E-02 3
rs62256378
SUCLG2
0.925 0.080 3 67406609 intron variant G/A;C snv 3
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs17641411
GABRA4
4 46941670 intron variant C/T snv 2.8E-02 1
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25