rs118203345
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs118203345
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs118203345
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013
rs118203345
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs118203345
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs118203396
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs118203396
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs118203396
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs118203396
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013
rs118203396
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs118203426
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013
rs118203436
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs118203436
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013
rs118203436
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs118203436
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs118203436
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs749030456
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
FOCAL CORTICAL DYSPLASIA OF TAYLOR
0.800
GeneticVariation
UNIPROT
Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
28215400
2017
rs75820036
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs75820036
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs75820036
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs75820036
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013
rs75820036
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs1060505021
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
FOCAL CORTICAL DYSPLASIA OF TAYLOR
0.700
GeneticVariation
UNIPROT
Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
28215400
2017
rs118203342
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.700
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs118203342
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
TUBEROUS SCLEROSIS 1 (disorder)
0.700
GeneticVariation
UNIPROT
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
23519317
2013