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: rs45517393
rs45517393
TSC2
1 1.000 0.120 16 2088105 missense variant C/G;T snv 0.800 1.000 20 1996 2013
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: rs45438205
rs45438205
TSC2
2 0.925 0.120 16 2080365 missense variant C/T snv 7.0E-06 0.800 1.000 13 1996 2017
dbSNP: rs45507199
rs45507199
PKD1 ; TSC2
3 0.925 0.120 16 2088294 missense variant G/A;C;T snv 0.800 1.000 13 1998 2017
dbSNP: rs45517214
rs45517214
TSC2
1 1.000 0.120 16 2072293 missense variant T/A;G snv 0.800 0
dbSNP: rs45517275
rs45517275
TSC2
1 1.000 0.120 16 2077647 missense variant G/A snv 2.0E-05 4.2E-05 0.700 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: rs45517294
rs45517294
TSC2
1 1.000 0.120 16 2080197 missense variant G/A;T snv 2.4E-04 0.700 1.000 20 1996 2017
dbSNP: rs45517418
rs45517418
PKD1 ; TSC2
1 1.000 0.120 16 2088504 missense variant A/C;G snv 8.0E-06 0.700 1.000 20 1996 2017
dbSNP: rs777166275
rs777166275
PKD1 ; TSC2
1 1.000 0.120 16 2088533 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.700 1.000 20 1996 2017
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: rs45459299
rs45459299
PKD1 ; TSC2
1 1.000 0.120 16 2088314 missense variant C/T snv 4.0E-06 0.700 1.000 16 1996 2005
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