Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 11
rs76980269
NOS1
0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs72824905
PLCG2
0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 5
rs762046989
MAPT
0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 5
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 4
rs1768208
MOBP
0.851 0.200 3 39481512 intron variant T/C snv 0.76 4
rs2471738
STH ; MAPT
0.882 0.160 17 45998697 intron variant C/T snv 0.18 4
rs4239633
UNC13A
0.851 0.240 19 17631660 intron variant C/T snv 0.32 4
rs13302855 0.882 0.200 9 27595997 intergenic variant C/T snv 7.5E-02 3
rs1026683055
GRN
0.882 0.200 17 44351429 missense variant C/T snv 1.6E-05 1.5E-05 3
rs1816
KANSL1
0.882 0.200 17 46199252 intron variant A/G snv 0.14 3
rs63751391
MAPT
0.882 0.120 17 46010395 missense variant G/T snv 3