Source: CLINVAR

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 14
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 4
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 3
rs57318642
LMNA
0.851 0.200 1 156137203 missense variant C/T snv 1.4E-05 1.4E-05 3
rs267607591
LMNA
0.882 0.200 1 156135274 missense variant G/A snv 1
rs57920071
LMNA
0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 1