Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs121434491
EFEMP1 ; LOC112268416
0.752 0.200 2 55871091 missense variant G/A snv 15
rs11200638
LOC105378525 ; HTRA1
0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs121908150
NLRP3
0.851 0.080 1 247424227 stop gained C/T snv 5
rs763544450
ERG
1.000 0.080 21 38445560 missense variant T/G snv 4.0E-06 4
rs1177783734
LOC101929066 ; ASAH1
0.925 0.080 8 18083991 missense variant T/G snv 4.5E-06 7.0E-06 4
rs1438303929
LOC102724808 ; OPA1
3 193647145 missense variant G/A snv 1.2E-05 1
rs756535079
SPG7
16 89544732 missense variant G/A;T snv 8.0E-06 7.0E-06 1
rs17822656
ZPLD1
3 102470325 intron variant T/C snv 9.5E-02 1