rs1555404803
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
|
31730815 |
2020 |
rs1566896114
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
|
31730815 |
2020 |
rs1566913670
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
|
31730815 |
2020 |
rs1555399165
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1555400274
|
|
GT |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566891645
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566895225
|
|
TC |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566896114
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566898399
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566904011
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566906537
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566908956
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566909766
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566915335
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566919599
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1566937712
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs397515765
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs397515784
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs397515819
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs794728208
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
|
30675029 |
2019 |
rs1064794282
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The importance of genotype-phenotype correlation in the clinical management of Marfan syndrome.
|
29357934 |
2018 |
rs113001196
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The importance of genotype-phenotype correlation in the clinical management of Marfan syndrome.
|
29357934 |
2018 |
rs1057518881
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
FBN1 mutations largely contribute to sporadic non-syndromic aortic dissection.
|
28973303 |
2017 |
rs1060501017
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Evaluating the quality of Marfan genotype-phenotype correlations in existing FBN1 databases.
|
27906200 |
2017 |
rs140597
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A cohort study of multiple families with FBN1 p.R650C variant, ectopia lentis, and low but not absent risk for aortopathy.
|
28941062 |
2017 |