Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607594
LMNA
0.925 0.120 1 156130745 missense variant T/C snv 3
rs267607639
LMNA
0.882 0.200 1 156136939 missense variant T/C snv 3
rs28928901
LMNA
0.882 0.120 1 156134829 missense variant C/T snv 3
rs28933090
LMNA
0.925 0.160 1 156115172 missense variant T/A;G snv 3
rs58850446
LMNA
0.925 0.200 1 156134908 missense variant T/C snv 3
rs60934003
LMNA
0.882 0.160 1 156137213 missense variant T/C snv 3
rs267607613
LMNA
0.925 0.120 1 156137678 missense variant C/T snv 7.0E-06 2
rs267607634
LMNA
0.925 0.120 1 156136045 missense variant G/A;C snv 2
rs267607637
LMNA
0.925 0.120 1 156136402 missense variant G/A snv 2
rs56771886
LMNA
0.925 0.160 1 156135923 frameshift variant T/- delins 2
rs57207746
LMNA
0.925 0.120 1 156134860 missense variant G/A snv 2
rs57747780
LMNA
0.925 0.200 1 156136981 missense variant T/C snv 2
rs58048078
LMNA
0.925 0.120 1 156134942 stop gained T/A;C snv 4.0E-06 2
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
rs58917027
LMNA
1.000 0.120 1 156130708 missense variant A/C;G snv 2
rs59653062
LMNA
0.925 0.120 1 156136076 missense variant T/A snv 2
rs60695352
LMNA
0.925 0.120 1 156115067 splice donor variant G/A;C;T snv 9.5E-06 2
rs61046466
LMNA
1.000 0.120 1 156114934 stop gained C/T snv 2
rs61094188
LMNA
0.925 0.160 1 156136257 missense variant C/A;T snv 7.6E-05 2
rs61295588
LMNA
0.925 0.160 1 156134809 missense variant T/C snv 2
rs797045011
LMNA
0.925 0.160 1 156135314 splice donor variant T/C snv 2
rs13768
LMNA
1.000 0.120 1 156138660 missense variant G/A;T snv 2.4E-05 1
rs1553265999
LMNA
1.000 0.120 1 156136925 missense variant A/C snv 1
rs267607539
LMNA
1.000 0.120 1 156137237 splice region variant G/A;C snv 1