SNP Detail For rs7873102
1.Mapping Information
Human SNP ID rs7873102
Human chromosome chr9
Human SNP position 38041145
Pig chromosome chr1
Pig SNP position 266814379
2.Annotation Information
PubMed ID20171287
JournalNeuroimage
Linkwww.ncbi.nlm.nih.gov/pubmed/20171287
StudyVoxelwise genome-wide association study (vGWAS).
Disease/TraitBrain structure
Initial sample740 European ancestry individuals
Replication sampleNA
Region9p13.1
Chromosome idchr9
Chromosome position38041145
Reported geneSHB
Mapped geneSHB
Upstream gene id
Downstream gene id
SNP gene ids6461
Upstream gene distance
Downstream gene distance
SNP risk allelers7873102-?
SNPsrs7873102
Merged0
SNP id current7873102
Contextintron_variant
Intergenic0
Allele frequency0.38
P value0.0000006
Pvalue mlog6.22184874961635
P value text
Or beta
%95 Ci
PlatformIllumina [448293]
CNVN
Mapped traitbrain measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004464
Study accessionGCST000597