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
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs114925667
NPHP3-ACAD11 ; UBA5
0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs113994095
POLG ; MIR6766
0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1064797245
ATP1A3
0.776 0.280 19 41970540 missense variant G/A snv 12
rs143319805
OPA1
0.807 0.320 3 193643378 missense variant A/G snv 6.2E-04 5.7E-04 12
rs796052676
KCNQ3
0.807 0.200 8 132180246 missense variant G/A snv 10
rs74315403
PRNP
0.790 0.200 20 4699752 missense variant G/A snv 10
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs118192211
KCNQ2
0.790 0.080 20 63439644 missense variant G/A;C snv 9
rs587776983
TUBB4A
0.807 0.240 19 6502209 missense variant G/A;C;T snv 9
rs1799821
CPT2
0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs2229291
CPT2
0.827 0.200 1 53210729 missense variant T/G snv 2.3E-02 1.5E-02 8
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs745386663
GLB1
0.807 0.160 3 33051956 missense variant G/A snv 8.0E-06 2.1E-05 7
rs886041715
GNAO1 ; DKFZP434H168 ; LOC283856
0.827 0.040 16 56192353 missense variant G/A;C;T snv 7
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs796052621
KCNQ2
0.827 0.080 20 63444756 missense variant C/T snv 6