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
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
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
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 9
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs150840924
LMNA
0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 7
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs4641
LMNA
0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs56657623
LMNA
0.827 0.120 1 156138540 missense variant G/A snv 1.6E-05 7.0E-06 5
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs1553265736
LMNA
0.925 0.040 1 156136080 missense variant G/C snv 4
rs267607571
LMNA
0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs267607581
LMNA
0.925 0.080 1 156137651 splice region variant C/G snv 4
rs28933091
LMNA
0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs56816490
LMNA
0.925 0.120 1 156135913 stop gained G/A;T snv 4
rs59301204
LMNA
0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4