SNP Detail For rs10007186
1.Mapping Information
Human SNP ID rs10007186
Human chromosome chr4
Human SNP position 78667891
Pig chromosome chr8
Pig SNP position 148076787
2.Annotation Information
PubMed ID22558069
JournalPLoS One
Linkwww.ncbi.nlm.nih.gov/pubmed/22558069
StudyAssociation of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
Disease/TraitNon-albumin protein levels
Initial sampleUp to 9,103 Japanese ancestry individuals
Replication sampleUp to 1,629 Japanese ancestry individuals
Region4q21.21
Chromosome idchr4
Chromosome position78667891
Reported geneANXA3
Mapped geneLINC01094
Upstream gene id
Downstream gene id
SNP gene ids100505702
Upstream gene distance
Downstream gene distance
SNP risk allelers10007186-C
SNPsrs10007186
Merged0
SNP id current10007186
Contextintron_variant
Intergenic0
Allele frequency0.307
P value0.000000001
Pvalue mlog9
P value text(NAP)
Or beta0.085
%95 Ci[0.058-0.112] unit increase
PlatformIllumina [2178644] (imputed)
CNVN
Mapped traitserum non-albumin protein measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004568
Study accessionGCST001496