Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs58932704
rs58932704
LMNA
8 0.776 0.200 1 156136413 missense variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs267607632
rs267607632
LMNA
4 0.851 0.120 1 156134976 splice donor variant G/A;C snv 0.700 0
dbSNP: rs386134243
rs386134243
LMNA
16 0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs60682848
rs60682848
LMNA
11 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 0.700 0
dbSNP: rs61672878
rs61672878
LMNA
11 0.776 0.200 1 156136094 missense variant G/A;T snv 0.020 0.500 2 2002 2016
dbSNP: rs58048078
rs58048078
LMNA
2 0.925 0.120 1 156134942 stop gained T/A;C snv 4.0E-06 0.010 1.000 1 2003 2003