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
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs863225264
MTOR
0.827 0.240 1 11130747 missense variant C/T snv 6
rs886041761
KCNA2
0.925 0.200 1 110603902 missense variant C/T snv 6
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 4
rs115466046
KCNJ10
1 160042480 missense variant C/T snv 1.2E-02 1.1E-02 2
rs140646329
KCNJ10
1 160042283 missense variant C/T snv 2.0E-05 1.4E-05 2
rs864309721
CDC42
1.000 1 22086451 missense variant A/G snv 2
rs374073809
VASH2
1 212961166 missense variant C/A;G;T snv 4.0E-06; 1.6E-05; 3.2E-05 1
rs753303079
CD55
1 207325673 missense variant C/G;T snv 8.0E-06 1
rs930549037
COL9A2
1 40301333 missense variant C/T snv 4.4E-05 2.8E-05 1
rs387906799
KIF1A
0.742 0.200 2 240788118 missense variant G/A snv 19
rs587777570
KIF5C
1.000 2 148947018 missense variant G/A snv 4
rs869320632
LMAN2L
0.925 0.040 2 96739883 missense variant C/T snv 4
rs781442277
PTRHD1 ; CENPO ; LOC105369164
1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs745756308
HNMT ; LOC107985948
1.000 2 138013874 missense variant T/C snv 4.0E-06 2
rs758252808
HNMT
1.000 2 137970206 missense variant G/A snv 4.1E-06 2
rs768560449
IMMT
1.000 0.160 2 86166521 missense variant A/G snv 8.1E-06 7.0E-06 2
rs10194776
PSMD1 ; HTR2B
2 231115305 intron variant C/T snv 0.54 1
rs1171889657
HADHB
2 26273656 missense variant T/C snv 4.0E-06 1
rs16827801
PSMD1 ; HTR2B
2 231116063 intron variant A/C;G snv 0.40 1