SNP Detail For rs5910578
1.Mapping Information
Human SNP ID rs5910578
Human chromosome chrX
Human SNP position 119433739
Pig chromosome chrX
Pig SNP position 113765376
2.Annotation Information
PubMed ID21623375
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21623375
StudyGenome-wide association identifies three new susceptibility loci for Paget__s disease of bone.
Disease/TraitPaget__s disease
Initial sample741 European ancestry cases, 2,699 European ancestry controls
Replication sample1,474 European ancestry cases, 1,671 European ancestry controls
RegionXq24
Chromosome idchrX
Chromosome position119433739
Reported geneSLC25A43
Mapped geneSLC25A43
Upstream gene id
Downstream gene id
SNP gene ids203427
Upstream gene distance
Downstream gene distance
SNP risk allelers5910578-C
SNPsrs5910578
Merged0
SNP id current5910578
Contextintron_variant
Intergenic0
Allele frequency0.74
P value0.0000001
Pvalue mlog7
P value text
Or beta1.34
%95 Ci[NR]
PlatformIllumina [2487078] (imputed)
CNVN
Mapped traitosteitis deformans
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004261
Study accessionGCST001086