Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs1800014
PRNP
0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs74315403
PRNP
0.790 0.200 20 4699752 missense variant G/A snv 10
rs11538758
PRNP
0.882 0.160 20 4699534 missense variant C/A;T snv 8
rs2986017
CALHM1
0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs74315405
PRNP
0.827 0.160 20 4699813 missense variant T/C snv 6
rs74315412
PRNP
0.851 0.120 20 4699843 missense variant G/A snv 6.0E-05 3.5E-05 5
rs773268484
AQP1
0.851 0.120 7 30922174 frameshift variant G/- delins 4.0E-06 7.0E-06 4
rs386747134
CALHM1
0.882 0.120 10 103458495 missense variant AGC/GGT mnv 3
rs760832624
CALHM1
0.882 0.120 10 103458488 frameshift variant CAGCGGCC/- delins 3
rs2245220
PRND
0.882 0.160 20 4725072 missense variant C/G;T snv 4.1E-06; 0.46 0.52 3
rs766487967
NPRL3 ; MPG
1.000 0.120 16 85517 missense variant G/A snv 8.0E-06 5.6E-05 2
rs2986018
CALHM1
1.000 0.120 10 103458602 synonymous variant T/C snv 0.81 0.83 1
rs41287500
CALHM1
1.000 0.120 10 103455334 missense variant C/A;T snv 2.0E-05; 1.6E-02 1
rs41287502
CALHM1
1.000 0.120 10 103455459 missense variant C/A snv 1.6E-02 1.7E-02 1
rs4918016
CALHM1
1.000 0.120 10 103458497 synonymous variant C/A;T snv 0.34 1
rs1029273
RPS4XP2
1.000 0.120 20 4675114 intron variant C/G;T snv 1