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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs12752888
LINC02784
0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 4
rs63750048
PSEN2
0.925 0.080 1 226883817 missense variant C/T snv 4.0E-06 2
rs774321998
C1orf167 ; MTHFR
1.000 0.040 1 11790683 missense variant T/C snv 4.0E-06 7.0E-06 1
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs12053868
IL1RAP
0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs3796529
REST
0.925 0.080 4 56931248 missense variant C/T snv 0.22 0.22 3
rs6850306
LCORL
0.925 0.080 4 18004466 intron variant G/A snv 0.12 2
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs111943087
CSF1R
0.925 0.080 5 150059725 missense variant G/A snv 1.4E-05 2
rs15009
PLK2
0.925 0.080 5 58454523 3 prime UTR variant C/G snv 0.37 2
rs3756577
CAMK2A
0.925 0.080 5 150249081 intron variant C/T snv 0.14 2
rs3822606
CAMK2A
0.925 0.080 5 150261592 intron variant G/A snv 0.27 2
rs702723
PLK2
0.925 0.080 5 58457629 non coding transcript exon variant C/T snv 0.67 0.66 2
rs640476 1.000 0.040 5 161277998 intergenic variant T/G snv 0.42 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4