SNP Detail For rs6991952
1.Mapping Information
Human SNP ID rs6991952
Human chromosome chr8
Human SNP position 25849896
Pig chromosome chr14
Pig SNP position 10990141
2.Annotation Information
PubMed ID26686553
JournalNat Commun
Linkwww.ncbi.nlm.nih.gov/pubmed/26686553
StudyA genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia.
Disease/TraitInguinal hernia
Initial sample5,295 European ancestry cases, 67,510 European ancestry controls
Replication sample9,701 European ancestry cases, 82,743 European ancestry controls
Region8p21.2
Chromosome idchr8
Chromosome position25849896
Reported geneEBF2
Mapped geneLOC102723395, EBF2
Upstream gene id
Downstream gene id
SNP gene ids102723395, 64641
Upstream gene distance
Downstream gene distance
SNP risk allelers6991952-G
SNPsrs6991952
Merged
SNP id current6991952
Contextintron_variant
Intergenic0
Allele frequency0.43
P value0.000000000000007
Pvalue mlog14.1549019599857
P value text
Or beta1.11
%95 Ci[1.08-1.14]
PlatformAffymetrix [6161781] (imputed)
CNVN
Mapped trait
Mapped trait URI
Study accessionGCST003198