rs28935480
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Structural Basis for Properdin Oligomerization and Convertase Stimulation in the Human Complement System.
|
31507604 |
2019 |
rs28935480
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Functional and structural insight into properdin control of complement alternative pathway amplification.
|
28264884 |
2017 |
rs28935480
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
|
10909851 |
2000 |
rs28935480
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutations.
|
9710744 |
1998 |
rs28935480
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.
|
8871668 |
1996 |
rs28935480
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs132630259
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Structural Basis for Properdin Oligomerization and Convertase Stimulation in the Human Complement System.
|
31507604 |
2019 |
rs132630261
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Structural Basis for Properdin Oligomerization and Convertase Stimulation in the Human Complement System.
|
31507604 |
2019 |
rs132630259
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Functional and structural insight into properdin control of complement alternative pathway amplification.
|
28264884 |
2017 |
rs132630261
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Functional and structural insight into properdin control of complement alternative pathway amplification.
|
28264884 |
2017 |
rs132630259
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
|
10909851 |
2000 |
rs132630261
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.
|
10909851 |
2000 |
rs132630259
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutations.
|
9710744 |
1998 |
rs132630261
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Expression of properdin in complete and incomplete deficiency: normal in vitro synthesis by monocytes in two cases with properdin deficiency type II due to distinct mutations.
|
9710744 |
1998 |
rs132630259
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.
|
8871668 |
1996 |
rs132630261
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.
|
8871668 |
1996 |
rs132630258
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs132630260
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|