SNP Detail For rs6137726
1.Mapping Information
Human SNP ID rs6137726
Human chromosome chr20
Human SNP position 22691782
Pig chromosome chr17
Pig SNP position 34125380
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
Region20p11.21
Chromosome idchr20
Chromosome position22691782
Reported geneSSTR4
Mapped geneLOC105372566 - KRT18P3
Upstream gene id105372566
Downstream gene id170527
SNP gene ids
Upstream gene distance5088
Downstream gene distance40951
SNP risk allelers6137726-?
SNPsrs6137726
Merged0
SNP id current6137726
Contextintron_variant
Intergenic1
Allele frequency
P value0.0000009
Pvalue mlog6.04575749056067
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