Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs119103263
MFN2
0.827 0.240 1 11992659 missense variant C/T snv 17
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 14
rs137852973
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 5
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5
rs119103268
MFN2
0.827 0.080 1 11992689 missense variant C/T snv 5
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 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
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 4
rs57629361
LMNA
0.827 0.280 1 156137207 missense variant C/A;G;T snv 9.3E-06 4
rs58596362
LMNA
0.827 0.280 1 156138613 splice region variant C/A;T snv 8.1E-06 4
rs58932704
LMNA
0.776 0.200 1 156136413 missense variant C/T snv 4
rs59885338
LMNA
0.851 0.120 1 156135268 missense variant C/T snv 3.6E-05 2.8E-05 4
rs60458016
LMNA
0.827 0.120 1 156136036 stop gained G/A;T snv 4
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 4
rs60864230
LMNA
0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 4
rs119103267
MFN2
0.790 0.160 1 12009641 missense variant C/T snv 2.5E-04 2.8E-04 4
rs28940292
MFN2
0.851 0.080 1 12011510 missense variant G/C snv 4
rs773159585
MFN2
0.882 0.080 1 11998877 missense variant C/T snv 8.0E-06 4
rs267606621
AARS1
0.882 0.080 16 70268356 missense variant C/T snv 3
rs137852972
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 3
rs587777606
HNRNPUL2-BSCL2 ; BSCL2 ; LRRN4CL
0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 3
rs121912496
LMNA
0.882 0.120 1 156134910 missense variant C/G;T snv 3
rs267607578
LMNA
0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 3