Gene: TSC2 ×
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: rs397515225
rs397515225
TSC2
1 1.000 0.120 16 2080366 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs45517305
rs45517305
TSC2
5 0.851 0.240 16 2081646 stop gained C/A;T snv 0.010 1.000 1 1998 1998
dbSNP: rs993614997
rs993614997
TSC2
1 1.000 0.120 16 2081714 missense variant C/T snv 2.1E-05 0.010 1.000 1 2012 2012
dbSNP: rs45517308
rs45517308
TSC2
2 0.925 0.120 16 2081734 stop gained C/A;G;T snv 8.0E-06 0.700 1.000 4 2001 2017
dbSNP: rs397514916
rs397514916
TSC2
2 0.925 0.120 16 2083754 missense variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1459518095
rs1459518095
TSC2
1 1.000 0.120 16 2084552 missense variant C/G;T snv 4.2E-06 0.010 1.000 1 2012 2012
dbSNP: rs45516293
rs45516293
TSC2
2 0.925 0.120 16 2084965 missense variant A/C;G snv 0.700 1.000 4 2001 2013
dbSNP: rs137854329
rs137854329
TSC2
1 1.000 0.120 16 2085238 frameshift variant -/T delins 0.700 0
dbSNP: rs1567533189
rs1567533189
TSC2
2 0.925 0.160 16 2086283 frameshift variant AAGGACTGCCA/- del 0.700 1.000 1 2019 2019
dbSNP: rs45517382
rs45517382
TSC2
2 0.925 0.120 16 2086834 missense variant A/G snv 0.700 0
dbSNP: rs45483392
rs45483392
TSC2
2 0.925 0.120 16 2087897 missense variant C/A;T snv 0.700 0
dbSNP: rs137854218
rs137854218
PKD1 ; TSC2
3 0.925 0.120 16 2088293 inframe insertion CATCAAGCGGCTCCGCCA/-;CATCAAGCGGCTCCGCCACATCAAGCGGCTCCGCCA delins 0.700 0
dbSNP: rs45507199
rs45507199
PKD1 ; TSC2
3 0.925 0.120 16 2088294 missense variant G/A;C;T snv 0.700 1.000 9 1998 2016
dbSNP: rs45517423
rs45517423
PKD1 ; TSC2
1 1.000 0.120 16 2088569 missense variant C/T snv 1.5E-03 1.5E-03 0.010 1.000 1 2008 2008