rs1013579
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs12085435
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs12085435
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Invasive meningococcal disease
|
|
0.010 |
GeneticVariation |
BEFREE |
The association between C8B rs12085435 and IMD requires independent replication.
|
25798599 |
2015 |
rs12092641
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs140813121
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs146187042
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Complement Component 6 Deficiency
|
A |
0.700 |
CausalMutation |
CLINVAR |
[Further study on heterogeneic basis of complement C8 beta deficiency].
|
14767900 |
2004 |
rs146187042
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs146187042
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Complement Component 6 Deficiency
|
A |
0.700 |
CausalMutation |
CLINVAR |
Delineation of additional genetic bases for C8 beta deficiency. Prevalence of null alleles and predominance of C-->T transition in their genesis.
|
7594510 |
1995 |
rs146187042
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Complement Component 6 Deficiency
|
A |
0.700 |
CausalMutation |
CLINVAR |
A novel mutation in a patient with a deficiency of the eighth component of complement associated with recurrent meningococcal meningitis.
|
19434484 |
2009 |
rs150022116
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs3216676
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
GA |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs372968576
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs398122867
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs398122868
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
GCACAGCC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs41286844
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Complement Component 6 Deficiency
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic basis of human complement C8 beta deficiency.
|
8098723 |
1993 |
rs41286844
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Complement Component 6 Deficiency
|
A |
0.700 |
CausalMutation |
CLINVAR |
Delineation of additional genetic bases for C8 beta deficiency. Prevalence of null alleles and predominance of C-->T transition in their genesis.
|
7594510 |
1995 |
rs41286844
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs41452950
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs612563
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs618184
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs684782
|
Entrez Id: |
732 |
Gene Symbol: |
C8B |
C8B
|
Blood Protein Measurement
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs78501968
|
C8B;LOC105378745
|
Blood Protein Measurement
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |