SNP Detail For rs17767392
1.Mapping Information
Human SNP ID rs17767392
Human chromosome chr14
Human SNP position 71298060
Pig chromosome chr7
Pig SNP position 101011799
2.Annotation Information
PubMed ID26301497
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/26301497
StudyGenetic association analyses highlight biological pathways underlying mitral valve prolapse.
Disease/TraitMitral valve prolapse
Initial sample1,442 European ancestry cases, 2,439 European ancestry controls
Replication sample1,422 European ancestry cases, 6,779 European ancestry controls
Region14q24.2
Chromosome idchr14
Chromosome position71298060
Reported genePCNX, SIPA1L1
Mapped geneLOC102724015
Upstream gene id
Downstream gene id
SNP gene ids102724015
Upstream gene distance
Downstream gene distance
SNP risk allelers17767392-T
SNPsrs17767392
Merged
SNP id current17767392
Contextintron_variant
Intergenic0
Allele frequency0.25
P value0.00000002
Pvalue mlog7.69897000433601
P value text
Or beta1.23
%95 Ci[1.15-1.32]
PlatformAffymetrix, Illumina [~ 4800000] (imputed)
CNVN
Mapped traitMitral valve prolapse
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0001634
Study accessionGCST003094