SNP Detail For rs9270986
1.Mapping Information
Human SNP ID rs9270986
Human chromosome chr6
Human SNP position 32606283
Pig chromosome chr7
Pig SNP position 29139424
2.Annotation Information
PubMed ID25643325
JournalJAMA Neurol
Linkwww.ncbi.nlm.nih.gov/pubmed/25643325
StudyA Genome-wide Association Study of Myasthenia Gravis.
Disease/TraitMyasthenia gravis
Initial sample972 European ancestry cases, 1,977 European ancestry controls
Replication sample423 European ancestry cases, 467 European ancestry controls
Region6p21.32
Chromosome idchr6
Chromosome position32606283
Reported geneHLA-DRB1, HLA-DQA1
Mapped geneHLA-DRB1 - HLA-DQA1
Upstream gene id3123
Downstream gene id3117
SNP gene ids
Upstream gene distance16447
Downstream gene distance31113
SNP risk allelers9270986-A
SNPsrs9270986
Merged0
SNP id current9270986
Contextintron_variant
Intergenic1
Allele frequency0.15
P value0.00000006
Pvalue mlog7.22184874961635
P value text
Or beta1.43
%95 Ci[NR]
PlatformIllumina [8114394] (imputed)
CNVN
Mapped traitMyasthenia gravis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004991
Study accessionGCST002838