Source: BEFREE ×
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
5 0.776 0.200 1 156136413 missense variant C/T snv 0.810 1.000 1 2008 2017
dbSNP: rs28933091
rs28933091
LMNA
2 0.882 0.160 1 156134474 missense variant C/A;G snv 0.710 1.000 1 2001 2001
dbSNP: rs58034145
rs58034145
LMNA
10 0.827 0.160 1 156134830 missense variant A/C snv 0.710 1.000 1 2005 2005
dbSNP: rs59653062
rs59653062
LMNA
2 0.925 0.120 1 156136076 missense variant T/A snv 0.710 1.000 1 2006 2006
dbSNP: rs61672878
rs61672878
LMNA
9 0.776 0.200 1 156136094 missense variant G/A;T snv 0.710 1.000 1 2004 2004
dbSNP: rs267607594
rs267607594
LMNA
2 0.925 0.120 1 156130745 missense variant T/C snv 0.010 1.000 1 2008 2008
dbSNP: rs267607613
rs267607613
LMNA
1 0.925 0.120 1 156137678 missense variant C/T snv 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs28933090
rs28933090
LMNA
2 0.925 0.160 1 156115172 missense variant T/A;G snv 0.010 1.000 1 2001 2001