SNP Detail For rs2058350
1.Mapping Information
Human SNP ID rs2058350
Human chromosome chr12
Human SNP position 3804261
Pig chromosome chr5
Pig SNP position 68796012
2.Annotation Information
PubMed ID20125193
JournalEur J Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20125193
StudyCommon genetic variation and performance on standardized cognitive tests.
Disease/TraitCognitive performance
Initial sampleUp to 813 European ancestry individuals, up to 167 East Asian ancestry individuals, up to 7 Hispanic/Latin American individuals, up to 74 South Asian ancestry individuals
Replication sampleNA
Region12p13.32
Chromosome idchr12
Chromosome position3804261
Reported genePARP11
Mapped geneCRACR2A - PARP11
Upstream gene id84766
Downstream gene id57097
SNP gene ids
Upstream gene distance51061
Downstream gene distance4600
SNP risk allelers2058350-?
SNPsrs2058350
Merged0
SNP id current2058350
Contextintron_variant
Intergenic1
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(PC1)
Or beta
%95 Ci
PlatformIllumina [up to 563855]
CNVN
Mapped traitneuropsychological test
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003926
Study accessionGCST000579