rs11337012
|
Entrez Id: |
4025 |
Gene Symbol: |
LPO |
LPO
|
Blood Protein Measurement
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genomic atlas of the human plasma proteome.
|
29875488 |
2018 |
rs546552332
|
Entrez Id: |
4025 |
Gene Symbol: |
LPO |
LPO
|
Blood basophil count (lab test)
|
C |
0.700 |
GeneticVariation |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
rs116372990
|
LPO;LOC105371841
|
response to bronchodilator
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
|
26634245 |
2015 |
rs116372990
|
LPO;LOC105371841
|
Chronic Obstructive Airway Disease
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
|
26634245 |
2015 |
rs141829479
|
LPO;LOC105371841
|
Chronic Obstructive Airway Disease
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
|
26634245 |
2015 |
rs141829479
|
LPO;LOC105371841
|
response to bronchodilator
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
|
26634245 |
2015 |
rs8178393
|
Entrez Id: |
4025 |
Gene Symbol: |
LPO |
LPO
|
Chronic Obstructive Airway Disease
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
|
26634245 |
2015 |
rs8178393
|
Entrez Id: |
4025 |
Gene Symbol: |
LPO |
LPO
|
response to bronchodilator
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
|
26634245 |
2015 |
rs863225205
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
|
0.700 |
GeneticVariation |
UNIPROT |
MKS1 regulates ciliary INPP5E levels in Joubert syndrome.
|
26490104 |
2016 |
rs863225205
|
LPO;MKS1;LOC105371841
|
Familial aplasia of the vermis
|
A |
0.700 |
CausalMutation |
CLINVAR |
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.
|
26092869 |
2015 |
rs863225205
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutation spectrum of Meckel syndrome genes: one group of syndromes or several distinct groups?
|
19466712 |
2009 |
rs375170572
|
LPO;MKS1;LOC105371841
|
Familial aplasia of the vermis
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
|
17397051 |
2007 |
rs375170572
|
LPO;MKS1;LOC105371841
|
Meckel-Gruber syndrome
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
|
17397051 |
2007 |
rs386834046
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
|
17397051 |
2007 |
rs386834046
|
LPO;MKS1;LOC105371841
|
BARDET-BIEDL SYNDROME 13
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
|
17397051 |
2007 |
rs386834046
|
LPO;MKS1;LOC105371841
|
JOUBERT SYNDROME 28
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
|
17397051 |
2007 |
rs386834051
|
LPO;MKS1;LOC105371841
|
BARDET-BIEDL SYNDROME 13
|
TCCCGG |
0.700 |
GeneticVariation |
CLINVAR |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs386834051
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
TCCCGG |
0.700 |
GeneticVariation |
CLINVAR |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs386834051
|
LPO;MKS1;LOC105371841
|
JOUBERT SYNDROME 28
|
TCCCGG |
0.700 |
GeneticVariation |
CLINVAR |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs386834052
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
G |
0.700 |
GeneticVariation |
CLINVAR |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs386834052
|
LPO;MKS1;LOC105371841
|
BARDET-BIEDL SYNDROME 13
|
G |
0.700 |
GeneticVariation |
CLINVAR |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs386834052
|
LPO;MKS1;LOC105371841
|
JOUBERT SYNDROME 28
|
G |
0.700 |
GeneticVariation |
CLINVAR |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs863225205
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
|
0.700 |
GeneticVariation |
UNIPROT |
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.
|
16415886 |
2006 |
rs1555601787
|
LPO;MKS1;LOC105371841
|
JOUBERT SYNDROME 28
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555601787
|
LPO;MKS1;LOC105371841
|
Meckel syndrome type 1
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|