SNP Detail For rs2255811
1.Mapping Information
Human SNP ID rs2255811
Human chromosome chr7
Human SNP position 113082141
Pig chromosome chr18
Pig SNP position 35228027
2.Annotation Information
PubMed ID25961943
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25961943
StudyThe impact of low-frequency and rare variants on lipid levels.
Disease/TraitTriglycerides
Initial sampleup to 62,166 European ancestry individuals
Replication sampleNA
Region7q31.1
Chromosome idchr7
Chromosome position113082141
Reported geneGPR85
Mapped geneGPR85
Upstream gene id
Downstream gene id
SNP gene ids54329
Upstream gene distance
Downstream gene distance
SNP risk allelers2255811-G
SNPsrs2255811
Merged
SNP id current2255811
Context3_prime_UTR_variant
Intergenic0
Allele frequency0.25
P value0.00000002
Pvalue mlog7.69897000433601
P value text
Or beta0.041
%95 Ci[0.027-0.055] s.d. increase
PlatformAffymetrix, Illumina, Perlegen [up to 9657952] (imputed)
CNVN
Mapped traittriglyceride measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004530
Study accessionGCST002897