SNP Detail For rs7148498
1.Mapping Information
Human SNP ID rs7148498
Human chromosome chr14
Human SNP position 95641618
Pig chromosome chr7
Pig SNP position 124097971
2.Annotation Information
PubMed ID24529757
JournalNeurobiol Aging
Linkwww.ncbi.nlm.nih.gov/pubmed/24529757
StudyGenome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Disease/TraitAmyotrophic lateral sclerosis (sporadic)
Initial sample250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls
Replication sampleNA
Region14q32.13
Chromosome idchr14
Chromosome position95641618
Reported geneGLRX5
Mapped geneLOC105370643 - TCL6
Upstream gene id105370643
Downstream gene id27004
SNP gene ids
Upstream gene distance50628
Downstream gene distance9560
SNP risk allelers7148498-?
SNPsrs7148498
Merged0
SNP id current7148498
Contextintron_variant
Intergenic1
Allele frequency
P value0.000001
Pvalue mlog6
P value text
Or beta
%95 Ci
PlatformIllumina [859311]
CNVN
Mapped traitsporadic amyotrophic lateral sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001357
Study accessionGCST002337