Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 4
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs1859788
PILRA
0.925 0.080 7 100374211 missense variant A/C;G snv 4.0E-06; 0.65 3
rs8063
UBE2I
1.000 0.040 16 1324817 3 prime UTR variant A/C;G snv 4.0E-06; 4.0E-06; 0.71 1
rs4837766
CDK5RAP2
0.925 0.080 9 120402006 intron variant A/C;G;T snv 2
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs754203
CYP46A1
0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 3
rs11218304
LOC105369535 ; SORL1
0.925 0.080 11 121478402 intron variant A/G snv 0.30 2
rs12053868
IL1RAP
0.925 0.080 3 190582215 intron variant A/G snv 8.0E-02 2
rs35445101
HLA-DRB1
0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02 2
rs6598008
CDHR5
0.925 0.080 11 618172 intron variant A/G snv 0.48 2
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs10407447
PLD3
1.000 0.040 19 40363275 intron variant A/G snv 0.20 1
rs4829605 1.000 0.040 X 137182822 intergenic variant C/A;G snv 1
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13