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
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
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
rs137852972
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs28940291
MFN2
0.776 0.080 1 11992660 missense variant G/A snv 4.0E-06 9
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 8
rs58932704
LMNA
0.776 0.200 1 156136413 missense variant C/T snv 8
rs150840924
LMNA
0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 7
rs58596362
LMNA
0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 7
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs60864230
LMNA
0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 7
rs119103267
MFN2
0.790 0.160 1 12009641 missense variant C/T snv 2.5E-04 2.8E-04 7
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 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
rs119103268
MFN2
0.827 0.080 1 11992689 missense variant C/T snv 6
rs137852975
HNRNPUL2-BSCL2 ; BSCL2
0.851 0.240 11 62692671 stop gained C/A snv 2.0E-05 1.4E-05 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