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: rs45517258
rs45517258
TSC2
2 0.925 0.120 16 2076141 missense variant C/G;T snv 0.800 1.000 29 1996 2017
dbSNP: rs45517259
rs45517259
TSC2
3 0.925 0.120 16 2076142 missense variant G/A snv 0.800 1.000 27 1996 2017
dbSNP: rs45517382
rs45517382
TSC2
2 0.925 0.120 16 2086834 missense variant A/G snv 0.800 1.000 26 1996 2017
dbSNP: rs28934872
rs28934872
TSC2
5 0.851 0.200 16 2070571 missense variant G/A snv 0.800 1.000 25 1996 2016
dbSNP: rs45483392
rs45483392
TSC2
2 0.925 0.120 16 2087897 missense variant C/A;T snv 0.800 1.000 24 1996 2017
dbSNP: rs137854882
rs137854882
TSC2
1 1.000 0.120 16 2087941 missense variant G/A;C;T snv 0.800 1.000 20 1996 2017
dbSNP: rs45517286
rs45517286
TSC2
1 1.000 0.120 16 2079396 missense variant C/G;T snv 0.700 1.000 20 1996 2017
dbSNP: rs45517393
rs45517393
TSC2
1 1.000 0.120 16 2088105 missense variant C/G;T snv 0.800 1.000 20 1996 2013
dbSNP: rs137854875
rs137854875
TSC2
1 1.000 0.120 16 2056769 missense variant G/C snv 0.700 1.000 16 1996 2005
dbSNP: rs137854879
rs137854879
TSC2
1 1.000 0.120 16 2084715 missense variant G/A;C snv 0.700 1.000 16 1996 2005
dbSNP: rs397514916
rs397514916
TSC2
2 0.925 0.120 16 2083754 missense variant C/G;T snv 0.700 1.000 16 1996 2005
dbSNP: rs45454398
rs45454398
TSC2
1 1.000 0.120 16 2071511 missense variant C/A snv 0.700 1.000 16 1996 2005
dbSNP: rs45469298
rs45469298
TSC2
5 0.851 0.200 16 2070570 missense variant C/G;T snv 0.800 1.000 16 1996 2017
dbSNP: rs45486196
rs45486196
TSC2
2 1.000 0.120 16 2071924 missense variant G/A snv 0.700 1.000 16 1996 2005
dbSNP: rs45487497
rs45487497
TSC2
2 0.925 0.120 16 2058779 missense variant G/A snv 0.700 1.000 16 1996 2005
dbSNP: rs45497997
rs45497997
TSC2
1 1.000 0.120 16 2084712 missense variant C/G snv 0.700 1.000 16 1996 2005
dbSNP: rs45517122
rs45517122
TSC2
1 1.000 0.120 16 2056675 missense variant G/A snv 0.700 1.000 16 1996 2005
dbSNP: rs45517138
rs45517138
TSC2
1 1.000 0.120 16 2058773 missense variant T/C snv 0.700 1.000 16 1996 2005
dbSNP: rs45517147
rs45517147
TSC2
1 1.000 0.120 16 2060776 missense variant T/C snv 0.700 1.000 16 1996 2005
dbSNP: rs45517156
rs45517156
TSC2
1 1.000 0.120 16 2061970 missense variant T/G snv 0.700 1.000 16 1996 2005
dbSNP: rs45517236
rs45517236
TSC2
1 1.000 0.120 16 2074291 missense variant C/T snv 0.700 1.000 16 1996 2005
dbSNP: rs45517355
rs45517355
TSC2
1 1.000 0.120 16 2085306 missense variant A/G snv 0.700 1.000 16 1996 2005
dbSNP: rs45517380
rs45517380
TSC2
1 1.000 0.120 16 2086810 missense variant A/G;T snv 0.700 1.000 16 1996 2005
dbSNP: rs45517383
rs45517383
TSC2
1 1.000 0.120 16 2086840 missense variant C/T snv 0.700 1.000 16 1996 2005
dbSNP: rs45517413
rs45517413
PKD1 ; TSC2
1 1.000 0.120 16 2088297 missense variant T/C snv 0.700 1.000 16 1996 2005