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
rs374128662
SACS
0.925 0.160 13 23355798 missense variant G/A snv 1.6E-05 7.0E-06 2
rs1179247981
TSEN54 ; CASKIN2
1.000 0.080 17 75517041 missense variant A/T snv 2.1E-05 1