SNP Detail For rs11635553
1.Mapping Information
Human SNP ID rs11635553
Human chromosome chr15
Human SNP position 73457267
Pig chromosome chr7
Pig SNP position 64558419
2.Annotation Information
PubMed ID23382691
JournalPLoS Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23382691
StudyLoci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Disease/TraitIgG glycosylation
Initial sample2,247 European ancestry individuals
Replication sampleNA
Region15q24.1
Chromosome idchr15
Chromosome position73457267
Reported geneNR
Mapped geneREC114
Upstream gene id
Downstream gene id
SNP gene ids283677
Upstream gene distance
Downstream gene distance
SNP risk allelers11635553-G
SNPsrs11635553
Merged0
SNP id current11635553
Contextintron_variant
Intergenic0
Allele frequency0.992804206752874
P value0.000004
Pvalue mlog5.39794000867203
P value text(IGP74)
Or beta1.0812
%95 Ci[0.62-1.54] unit decrease
PlatformIllumina [~ 2500000] (imputed)
CNVN
Mapped traitserum IgG glycosylation measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005193
Study accessionGCST001848
PubMed ID23382691
JournalPLoS Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23382691
StudyLoci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Disease/TraitIgG glycosylation
Initial sample2,247 European ancestry individuals
Replication sampleNA
Region15q24.1
Chromosome idchr15
Chromosome position73457267
Reported geneNR
Mapped geneREC114
Upstream gene id
Downstream gene id
SNP gene ids283677
Upstream gene distance
Downstream gene distance
SNP risk allelers11635553-G
SNPsrs11635553
Merged0
SNP id current11635553
Contextintron_variant
Intergenic0
Allele frequency0.992814619440459
P value0.000006
Pvalue mlog5.22184874961635
P value text(IGP75)
Or beta1.0594
%95 Ci[0.6-1.52] unit decrease
PlatformIllumina [~ 2500000] (imputed)
CNVN
Mapped traitserum IgG glycosylation measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005193
Study accessionGCST001848
PubMed ID23382691
JournalPLoS Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23382691
StudyLoci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Disease/TraitIgG glycosylation
Initial sample2,247 European ancestry individuals
Replication sampleNA
Region15q24.1
Chromosome idchr15
Chromosome position73457267
Reported geneNR
Mapped geneREC114
Upstream gene id
Downstream gene id
SNP gene ids283677
Upstream gene distance
Downstream gene distance
SNP risk allelers11635553-G
SNPsrs11635553
Merged0
SNP id current11635553
Contextintron_variant
Intergenic0
Allele frequency0.99282491474212
P value0.000009
Pvalue mlog5.04575749056067
P value text(IGP76)
Or beta1.0357
%95 Ci[0.58-1.49] unit increase
PlatformIllumina [~ 2500000] (imputed)
CNVN
Mapped traitserum IgG glycosylation measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005193
Study accessionGCST001848