Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28928910
NEFL
0.827 0.200 8 24956452 missense variant G/A;T snv 11
rs58982919
NEFL
0.790 0.080 8 24956223 missense variant T/C snv 10
rs1059111
NEFL
0.827 0.200 8 24952575 3 prime UTR variant T/A;G snv 5
rs2979704
NEFL
0.827 0.200 8 24951554 3 prime UTR variant C/T snv 0.78 5
rs58332872
NEFL
0.882 0.080 8 24956248 missense variant C/T snv 5
rs57105105
NEFL ; MIR6841
0.925 0.080 8 24953776 missense variant C/T snv 4
rs60261494
NEFL
0.882 0.080 8 24956493 missense variant GG/CT mnv 3
rs62636503
NEFL ; MIR6841
0.882 0.080 8 24953779 missense variant C/T snv 3
rs267607538
NEFL
0.925 0.120 8 24956451 missense variant G/C;T snv 2
rs59101996
NEFL
0.925 0.080 8 24956070 missense variant G/A snv 2
rs61491953
NEFL
0.925 0.080 8 24956493 missense variant G/A;C;T snv 2
rs62636505
NEFL
0.925 0.080 8 24956235 missense variant A/G snv 2
rs281865140
NEFL ; MIR6841
0.925 0.080 8 24955515 missense variant T/C;G snv 2
rs59443585
NEFL ; MIR6841
0.925 0.080 8 24955521 missense variant T/G snv 2
rs587777881
MIR6841 ; NEFL
1.000 0.080 8 24955509 missense variant A/G snv 1
rs587777882
MIR6841 ; NEFL
1.000 0.080 8 24953646 missense variant G/A;C snv 1
rs757417962
MIR6841 ; NEFL
1.000 0.080 8 24954233 stop gained G/A;C snv 2.0E-05 7.0E-06 1
rs121913663
NEFL
1.000 0.080 8 24956098 stop gained C/A;T snv 4.2E-06; 4.2E-06 1
rs199422214
NEFL
1.000 0.080 8 24955888 stop gained C/A;G snv 1.7E-05 1
rs58640772
NEFL
1.000 0.080 8 24956455 frameshift variant -/TCCACGTAGCGCC delins 1
rs62636522
NEFL
1.000 0.080 8 24955877 missense variant G/A;C snv 4.1E-06; 7.2E-04 1
rs876661155
NEFL
1.000 0.080 8 24956029 stop gained C/A;G snv 1
rs1411999109
NEFL ; MIR6841
1.000 0.080 8 24955720 missense variant C/T snv 4.0E-06 1
rs191346286
NEFL ; MIR6841
1.000 0.080 8 24953704 stop gained G/A;T snv 4.4E-05 1
rs587777880
NEFL ; MIR6841
1.000 0.080 8 24955722 missense variant T/C snv 1