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
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
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
rs60864230
LMNA
0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 7
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
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs878853220
LMNA
0.827 0.200 1 156130818 intron variant T/G snv 6
rs57629361
LMNA
0.827 0.280 1 156137207 missense variant C/A;G;T snv 9.3E-06 5
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5
rs60458016
LMNA
0.827 0.120 1 156136036 stop gained G/A;T snv 5
rs60662302
LMNA
0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs267607571
LMNA
0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs267607632
LMNA
0.851 0.120 1 156134976 splice donor variant G/A;C snv 4
rs28933091
LMNA
0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs58327533
LMNA
1.000 0.120 1 156114991 missense variant C/G;T snv 4
rs60652225
LMNA
0.851 0.200 1 156130679 missense variant T/C;G snv 4
rs121912496
LMNA
0.882 0.120 1 156134910 missense variant C/G;T snv 3
rs267607545
LMNA
0.882 0.200 1 156136121 missense variant G/A;C;T snv 3