Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1352010373
TMEM94
0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1554317002
LOC112267983 ; CDK13
0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs1555735545
STRN4 ; FKRP
0.851 0.160 19 46746071 5 prime UTR variant G/A snv 22
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750852
PSEN1
0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs2732260
FUT10
0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 5
rs281865071
CHRNB2
0.882 0.080 1 154571759 missense variant C/G;T snv 5
rs8074995
PRKCA
0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs61748411
MECP2
0.925 0.120 X 154031356 missense variant T/C snv 3
rs1411832
LOC105378469
1.000 0.040 10 106126497 intergenic variant C/T snv 0.10 2
rs536551654
NGFR ; LOC100288866
1.000 0.120 17 49511972 missense variant T/C snv 2