Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs119103263
MFN2
0.827 0.240 1 11992659 missense variant C/T snv 19
rs137852973
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 13
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs58932704
LMNA
0.776 0.200 1 156136413 missense variant C/T snv 8
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs119103268
MFN2
0.827 0.080 1 11992689 missense variant C/T snv 6
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57983345
LMNA
0.851 0.160 1 156115034 missense variant A/G snv 6
rs59270054
LMNA
0.925 0.120 1 156115162 missense variant G/A;C snv 6
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs119103265
MFN2
0.827 0.120 1 12002033 missense variant C/T snv 5
rs121913598
MPZ
0.851 0.080 1 161307361 missense variant G/A snv 5
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5
rs60458016
LMNA
0.827 0.120 1 156136036 stop gained G/A;T snv 5
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs267607571
LMNA
0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs267607632
LMNA
0.851 0.120 1 156134976 splice donor variant G/A;C snv 4
rs28933091
LMNA
0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs28940292
MFN2
0.851 0.080 1 12011510 missense variant G/C snv 4
rs56816490
LMNA
0.925 0.120 1 156135913 stop gained G/A;T snv 4