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: rs118203490
rs118203490
TSC1
1 1.000 0.120 9 132911103 stop gained C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs367963898
rs367963898
TSC2
1 1.000 0.120 16 2060734 missense variant A/G snv 2.0E-05 7.0E-05 0.010 1.000 1 2019 2019
dbSNP: rs748011804
rs748011804
PIK3CD
1 1.000 0.120 1 9718800 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs780378198
rs780378198
TSC2
1 1.000 0.120 16 2060701 missense variant A/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs796053495
rs796053495
TSC2
1 1.000 0.120 16 2080195 missense variant A/T snv 4.0E-06 0.010 1.000 1 2019 2019
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
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: rs45517153
rs45517153
TSC2
1 1.000 0.120 16 2060687 missense variant C/A;T snv 1.6E-05 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: rs45517202
rs45517202
TSC2
1 1.000 0.120 16 2070535 missense variant A/G;T snv 4.0E-06 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