Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933091
LMNA
0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs56694480
LMNA
1.000 0.120 1 156115021 missense variant C/G snv 1
rs56699480
LMNA
1.000 0.120 1 156137017 stop gained C/T snv 1
rs56771886
LMNA
0.925 0.160 1 156135923 frameshift variant T/- delins 2
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57048196
LMNA
1.000 0.120 1 156134965 missense variant A/G snv 1
rs57207746
LMNA
0.925 0.120 1 156134860 missense variant G/A snv 2
rs57394692
LMNA
1.000 0.120 1 156136946 missense variant T/C snv 1
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 8
rs57629361
LMNA
0.827 0.280 1 156137207 missense variant C/A;G;T snv 9.3E-06 5
rs57747780
LMNA
0.925 0.200 1 156136981 missense variant T/C snv 2
rs57793737
LMNA
1.000 0.120 1 156115106 missense variant T/A;C;G snv 1
rs57983345
LMNA
0.851 0.160 1 156115034 missense variant A/G snv 6
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs58048078
LMNA
0.925 0.120 1 156134942 stop gained T/A;C snv 4.0E-06 2
rs58105277
LMNA
1.000 0.120 1 156135971 missense variant G/A snv 2.8E-05 1
rs58327533
LMNA
1.000 0.120 1 156114991 missense variant C/G;T snv 4
rs58362413
LMNA
0.925 0.160 1 156137183 stop gained G/A;C snv 2
rs58436778
LMNA
0.925 0.120 1 156115052 missense variant A/G snv 2
rs58541611
LMNA
1.000 0.120 1 156136393 missense variant A/G;T snv 1
rs58850446
LMNA
0.925 0.200 1 156134908 missense variant T/C snv 3
rs58917027
LMNA
1.000 0.120 1 156130708 missense variant A/C;G snv 2
rs58932704
LMNA
0.776 0.200 1 156136413 missense variant C/T snv 8
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5