Gene: LMNA ×
Source: INFERRED ×
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: rs267607578
rs267607578
LMNA
3 0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 0.810 1.000 8 1999 2014
dbSNP: rs56984562
rs56984562
LMNA
3 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.810 1.000 8 1999 2017
dbSNP: rs28933093
rs28933093
LMNA
3 0.882 0.160 1 156130741 missense variant G/A snv 0.810 1.000 0 1999 2012
dbSNP: rs267607570
rs267607570
LMNA
2 0.925 0.120 1 156130757 missense variant G/A;C snv 4.8E-05 0.800 1.000 0 1999 2017
dbSNP: rs28928900
rs28928900
LMNA
2 0.925 0.120 1 156115096 missense variant C/G;T snv 0.800 0
dbSNP: rs28933090
rs28933090
LMNA
1 0.925 0.160 1 156115172 missense variant T/A;G snv 0.800 1.000 0 1999 2017
dbSNP: rs28933091
rs28933091
LMNA
4 0.882 0.160 1 156134474 missense variant C/A;G snv 0.800 1.000 0 1999 2017
dbSNP: rs28933092
rs28933092
LMNA
2 1.000 0.040 1 156134497 missense variant A/G;T snv 0.800 1.000 0 1999 2012
dbSNP: rs60890628
rs60890628
LMNA
3 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 0.800 0
dbSNP: rs1057515421
rs1057515421
LMNA
1 0.925 0.120 1 156136284 stop gained C/T snv 0.700 1.000 2 1999 2016
dbSNP: rs11575937
rs11575937
LMNA
14 0.653 0.480 1 156136985 missense variant G/A;T snv 0.700 0
dbSNP: rs1165819867
rs1165819867
LMNA
1 1.000 0.040 1 156134892 missense variant G/A;T snv 0.700 0
dbSNP: rs1553265180
rs1553265180
LMNA
1 1.000 0.040 1 156134500 missense variant T/A;G snv 0.700 0
dbSNP: rs1553265736
rs1553265736
LMNA
4 0.925 0.040 1 156136080 missense variant G/C snv 0.700 0
dbSNP: rs1553265739
rs1553265739
LMNA
1 1.000 0.040 1 156136081 missense variant A/T snv 0.700 0
dbSNP: rs267607581
rs267607581
LMNA
4 0.925 0.080 1 156137651 splice region variant C/G 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: rs397517889
rs397517889
LMNA
3 0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs56771886
rs56771886
LMNA
2 0.925 0.160 1 156135923 frameshift variant T/- delins 0.700 0
dbSNP: rs57077886
rs57077886
LMNA
3 0.776 0.240 1 156114947 missense variant C/T snv 0.700 0
dbSNP: rs58362413
rs58362413
LMNA
1 0.925 0.160 1 156137183 stop gained G/A;C snv 0.700 0
dbSNP: rs59332535
rs59332535
LMNA
5 0.827 0.160 1 156134911 missense variant G/A snv 0.700 0
dbSNP: rs59684335
rs59684335
LMNA
3 0.882 0.120 1 156135280 frameshift variant CT/- delins 0.700 0
dbSNP: rs730882262
rs730882262
LMNA
3 0.851 0.160 1 156135293 missense variant T/C;G snv 0.700 0