Source: BEFREE

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
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 24
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 14
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
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 7
rs74315402
PRNP
0.882 0.200 20 4699570 missense variant C/T snv 6
rs16990018
PRNP
0.882 0.120 20 4699732 missense variant A/G snv 3.8E-03 1.6E-02 5
rs74315405
PRNP
0.827 0.160 20 4699813 missense variant T/C snv 5
rs1178466848
PRNP
0.925 0.120 20 4699785 missense variant G/A snv 2.8E-05 4
rs398122370
PRNP
0.925 0.160 20 4699851 missense variant G/C snv 4
rs74315412
PRNP
0.851 0.120 20 4699843 missense variant G/A snv 6.0E-05 3.5E-05 4
rs1191139947
PRNP
0.882 0.120 20 4699935 missense variant C/T snv 3
rs776593792
PRNP
1.000 0.120 20 4699827 missense variant G/A snv 1.6E-05 2.8E-05 2
rs181348299
PRNP
1.000 0.120 20 4699663 missense variant G/A snv 3.2E-05 1.4E-05 1
rs748929962
PRNP
1.000 0.120 20 4699894 missense variant A/G snv 4.0E-06 1
rs769346296
PRNP
1.000 0.120 20 4699807 missense variant A/C snv 6.0E-05 2.8E-05 1