SNP Detail For rs7322722
1.Mapping Information
Human SNP ID rs7322722
Human chromosome chr13
Human SNP position 77305241
Pig chromosome chr11
Pig SNP position 54091598
2.Annotation Information
PubMed ID23551011
JournalAnn Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23551011
StudyGenome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.
Disease/TraitPreeclampsia
Initial sample21 Afro-Caribbean cases, 1,010 Afro-Caribbean controls, 50 European ancestry cases, 1,202 European ancestry controls, 62 Hispanic cases, 658 Hispanic controls
Replication sampleNA
Region13q22.3
Chromosome idchr13
Chromosome position77305241
Reported geneMYCBP2
Mapped geneMYCBP2
Upstream gene id
Downstream gene id
SNP gene ids23077
Upstream gene distance
Downstream gene distance
SNP risk allelers7322722-?
SNPsrs7322722
Merged0
SNP id current7322722
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000001
Pvalue mlog6
P value text(EA)
Or beta2.93
%95 Ci[1.90-4.52]
PlatformIllumina [2485249] (imputed)
CNVN
Mapped traitpreeclampsia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000668
Study accessionGCST001949