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: rs57920071
rs57920071
LMNA
11 0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 0.100 1.000 14 2001 2018
dbSNP: rs11575937
rs11575937
LMNA
29 0.653 0.480 1 156136985 missense variant G/A;T snv 0.100 1.000 10 2000 2020
dbSNP: rs57830985
rs57830985
LMNA
2 0.925 0.080 1 156138534 missense variant G/A;T snv 8.2E-06 7.0E-06 0.020 1.000 2 2000 2000
dbSNP: rs72551364
rs72551364
PPARG
4 0.851 0.160 3 12433900 missense variant C/T snv 0.020 1.000 2 2002 2007
dbSNP: rs1057156731
rs1057156731
LMNA
3 0.925 0.120 1 156137730 missense variant T/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1354592503
rs1354592503
PPARG
2 0.925 0.120 3 12381463 missense variant A/G snv 1.4E-05 0.010 1.000 1 2011 2011
dbSNP: rs267607545
rs267607545
LMNA
3 0.882 0.200 1 156136121 missense variant G/A;C;T snv 0.010 1.000 1 2005 2005
dbSNP: rs267607608
rs267607608
LMNA
1 1.000 0.080 1 156115057 missense variant G/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs28928902
rs28928902
LMNA
4 0.851 0.160 1 156136951 missense variant C/G;T snv 1.2E-05 0.010 1.000 1 2007 2007
dbSNP: rs397517892
rs397517892
LMNA
4 0.851 0.240 1 156136419 missense variant C/T snv 9.9E-06 1.4E-05 0.010 1.000 1 2002 2002
dbSNP: rs56657623
rs56657623
LMNA
5 0.827 0.120 1 156138540 missense variant G/A snv 1.6E-05 7.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs57747780
rs57747780
LMNA
2 0.925 0.200 1 156136981 missense variant T/C snv 0.010 1.000 1 2001 2001
dbSNP: rs58932704
rs58932704
LMNA
8 0.776 0.200 1 156136413 missense variant C/T snv 0.010 1.000 1 2005 2005
dbSNP: rs61282106
rs61282106
LMNA
2 0.925 0.080 1 156136934 missense variant G/A snv 0.010 1.000 1 2003 2003
dbSNP: rs72551363
rs72551363
PPARG
3 0.882 0.080 3 12417048 missense variant T/A snv 0.010 1.000 1 2002 2002
dbSNP: rs770850320
rs770850320
SREBF1
3 0.882 0.120 17 17816960 missense variant G/A snv 2.0E-05 2.8E-05 0.010 1.000 1 2015 2015