Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 3
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 3
rs60652225
LMNA
0.851 0.200 1 156130679 missense variant T/C;G snv 2
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 2
rs60695352
LMNA
0.925 0.120 1 156115067 splice donor variant G/A;C;T snv 9.5E-06 2
rs60864230
LMNA
0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 2
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 2
rs57983345
LMNA
0.851 0.160 1 156115034 missense variant A/G snv 2
rs267607571
LMNA
0.882 0.160 1 156134458 missense variant G/A;T snv 2
rs121912496
LMNA
0.882 0.120 1 156134910 missense variant C/G;T snv 2
rs58672172
LMNA
0.882 0.160 1 156136251 missense variant C/T snv 1.2E-05 1.4E-05 2
rs28928900
LMNA
0.925 0.120 1 156115096 missense variant C/G;T snv 2
rs60310264
LMNA
0.827 0.200 1 156130693 missense variant G/A snv 1
rs58912633
LMNA
0.851 0.240 1 156130688 missense variant C/G;T snv 1
rs57318642
LMNA
0.851 0.200 1 156137203 missense variant C/T snv 1.4E-05 1.4E-05 1
rs79907212
LMNA
0.925 0.080 1 156135275 missense variant A/C;G snv 1
rs56673169
LMNA
0.925 0.160 1 156137671 missense variant G/C snv 1
rs267607649
LMNA
1.000 0.080 1 156130672 missense variant G/A snv 1
rs28928902
LMNA
0.851 0.160 1 156136951 missense variant C/G;T snv 1.2E-05 1
rs57207746
LMNA
0.925 0.120 1 156134860 missense variant G/A snv 1
rs267607614
LMNA
1.000 0.120 1 156115016 missense variant A/G snv 1
rs267607633
LMNA
1.000 0.120 1 156135259 missense variant T/C snv 1
rs28928901
LMNA
0.882 0.120 1 156134829 missense variant C/T snv 1
rs60662302
LMNA
0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 1
rs60992550
LMNA
1.000 0.120 1 156136423 missense variant A/T snv 1