SNP Detail For rs1049110
1.Mapping Information
Human SNP ID rs1049110
Human chromosome chr6
Human SNP position 32759026
Pig chromosome chr7
Pig SNP position 29244463
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
Region6p21.32
Chromosome idchr6
Chromosome position32759026
Reported geneHLA-DQA2, HLA-DQB2
Mapped geneHLA-DQB2
Upstream gene id
Downstream gene id
SNP gene ids3120
Upstream gene distance
Downstream gene distance
SNP risk allelers1049110-C
SNPsrs1049110
Merged0
SNP id current1049110
Contextmissense_variant
Intergenic0
Allele frequency0.34601888034188
P value0.00000004
Pvalue mlog7.39794000867203
P value text(IGP2)
Or beta0.1853
%95 Ci[0.12-0.25] unit increase
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
Region6p21.32
Chromosome idchr6
Chromosome position32759026
Reported geneHLA-DQA2, HLA-DQB2
Mapped geneHLA-DQB2
Upstream gene id
Downstream gene id
SNP gene ids3120
Upstream gene distance
Downstream gene distance
SNP risk allelers1049110-C
SNPsrs1049110
Merged0
SNP id current1049110
Contextmissense_variant
Intergenic0
Allele frequency0.346381764494382
P value0.00000002
Pvalue mlog7.69897000433601
P value text(IGP42)
Or beta0.1909
%95 Ci[0.12-0.26] unit increase
PlatformIllumina [~ 2500000] (imputed)
CNVN
Mapped traitserum IgG glycosylation measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005193
Study accessionGCST001848