Disease: Memory impairment
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5