SNP Detail For rs10502219
1.Mapping Information
Human SNP ID rs10502219
Human chromosome chr11
Human SNP position 116541896
Pig chromosome chr9
Pig SNP position 49031442
2.Annotation Information
PubMed ID25240745
JournalMitochondrion
Linkwww.ncbi.nlm.nih.gov/pubmed/25240745
StudyA genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.
Disease/TraitMitochondrial DNA levels
Initial sample173 European ancestry males and 213 European ancestry females from 21 families
Replication sampleNA
Region11q23.3
Chromosome idchr11
Chromosome position116541896
Reported geneMGC13125
Mapped geneLOC105369513 - LOC101929011
Upstream gene id105369513
Downstream gene id101929011
SNP gene ids
Upstream gene distance460840
Downstream gene distance97526
SNP risk allelers10502219-?
SNPsrs10502219
Merged0
SNP id current10502219
Contextintergenic_variant
Intergenic1
Allele frequencyNR
P value0.000006
Pvalue mlog5.22184874961635
P value text(Males)
Or beta
%95 Ci[NR]
PlatformIllumina [283437]
CNVN
Mapped traitmitochondrial DNA measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006312
Study accessionGCST002616