Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs281864720
ALK
0.925 0.040 2 29213994 missense variant A/C;G;T snv 4
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
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
rs143319805
OPA1
0.807 0.320 3 193643378 missense variant A/G snv 6.2E-04 5.7E-04 12
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs771844443
SCN2A
1.000 0.040 2 165309194 missense variant A/G snv 4.0E-06 3
rs796053150
SCN2A
1.000 0.040 2 165386827 missense variant A/G snv 3
rs866291718
LIAS
1.000 0.040 4 39470042 missense variant A/G snv 3
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs4945008
NADSYN1
1.000 0.080 11 71510202 intron variant A/G;T snv 2
rs1060499537
KCNT2
1.000 1 196429676 missense variant A/T snv 2
rs397514612
FARS2
1.000 6 5613275 missense variant A/T snv 1.6E-05 7.0E-06 2
rs756712426
IDH3A
15 78166196 missense variant C/A snv 2.0E-05 1
rs767399782
TUBB4A
0.925 0.120 19 6495736 missense variant C/A;T snv 4.0E-06 3
rs752874517
MIR6812 ; LOC105372631 ; PIGT
1.000 0.080 20 45425779 missense variant C/A;T snv 8.0E-06 7.0E-06 2
rs786203999
GPT2
1.000 16 46906858 missense variant C/G snv 2
rs756762431
TUBB4A
1.000 0.120 19 6495654 missense variant C/G;T snv 8.0E-06 2
rs886037942
SLC1A2
1.000 11 35315089 missense variant C/G;T snv 2
rs113994095
POLG ; MIR6766
0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs796052621
KCNQ2
0.827 0.080 20 63444756 missense variant C/T snv 6