SNP Detail For rs138206701
1.Mapping Information
Human SNP ID rs138206701
Human chromosome chr5
Human SNP position 81110747
Pig chromosome chr2
Pig SNP position 91588825
2.Annotation Information
PubMed ID23568457
JournalInt J Eat Disord
Linkwww.ncbi.nlm.nih.gov/pubmed/23568457
StudyGenetic variants associated with disordered eating.
Disease/TraitEating disorders (purging via substances)
Initial sample600 European ancestry female cases, 1,921 European ancestry female controls
Replication sampleNA
Region5q14.1
Chromosome idchr5
Chromosome position81110747
Reported geneRASGRF2
Mapped geneRASGRF2
Upstream gene id
Downstream gene id
SNP gene ids5924
Upstream gene distance
Downstream gene distance
SNP risk allelers138206701-A
SNPsrs138206701
Merged0
SNP id current138206701
Contextintron_variant
Intergenic0
Allele frequency0.98
P value0.0000001
Pvalue mlog7
P value text
Or beta0.327
%95 Ci[0.21-0.45] unit decrease
PlatformIllumina [6150213] (imputed)
CNVN
Mapped traiteating disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005203
Study accessionGCST001959
PubMed ID23568457
JournalInt J Eat Disord
Linkwww.ncbi.nlm.nih.gov/pubmed/23568457
StudyGenetic variants associated with disordered eating.
Disease/TraitEating disorders
Initial sample543 European ancestry female cases, 1,116 European ancestry female controls
Replication sampleNA
Region5q14.1
Chromosome idchr5
Chromosome position81110747
Reported geneRASGRF2
Mapped geneRASGRF2
Upstream gene id
Downstream gene id
SNP gene ids5924
Upstream gene distance
Downstream gene distance
SNP risk allelers138206701-A
SNPsrs138206701
Merged0
SNP id current138206701
Contextintron_variant
Intergenic0
Allele frequency0.98
P value0.000004
Pvalue mlog5.39794000867203
P value text
Or beta0.425
%95 Ci[0.24-0.61] unit decrease
PlatformIllumina [6150213] (imputed)
CNVN
Mapped traiteating disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005203
Study accessionGCST001960