Disease: Impaired cognition
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1345176461
LOC107984638 ; IRF2BPL
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs80358257
NPC1
0.827 0.280 18 23538564 missense variant G/C snv 1.2E-04 2.1E-04 8
rs372445155
NPC1
0.851 0.280 18 23554890 missense variant G/A snv 1.6E-05 2.1E-05 7