SNP Detail For rs11118844
1.Mapping Information
Human SNP ID rs11118844
Human chromosome chr1
Human SNP position 221736946
Pig chromosome chr10
Pig SNP position 13010885
2.Annotation Information
PubMed ID26451028
JournalStroke
Linkwww.ncbi.nlm.nih.gov/pubmed/26451028
StudyWhite Matter Lesion Progression: Genome-Wide Search for Genetic Influences.
Disease/TraitWhite matter lesion progression (adjusted for white matter lesion burden at baseline)
Initial sample1,085 European ancestry elderly cases, 6,688 European ancestry elderly controls
Replication sampleNA
Region1q41
Chromosome idchr1
Chromosome position221736946
Reported geneDUSP10
Mapped geneDUSP10
Upstream gene id
Downstream gene id
SNP gene ids11221
Upstream gene distance
Downstream gene distance
SNP risk allelers11118844-A
SNPsrs11118844
Merged
SNP id current11118844
Contextintron_variant
Intergenic0
Allele frequency0.86
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta1.49
%95 Ci[NR]
PlatformAffymetrix, Illumina [up to 2543887] (imputed)
CNVN
Mapped traitwhite matter lesion progression measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007746
Study accessionGCST003152
PubMed ID26451028
JournalStroke
Linkwww.ncbi.nlm.nih.gov/pubmed/26451028
StudyWhite Matter Lesion Progression: Genome-Wide Search for Genetic Influences.
Disease/TraitWhite matter lesion progression
Initial sample1,085 European ancestry elderly cases, 6,688 European ancestry elderly controls
Replication sampleNA
Region1q41
Chromosome idchr1
Chromosome position221736946
Reported geneDUSP10
Mapped geneDUSP10
Upstream gene id
Downstream gene id
SNP gene ids11221
Upstream gene distance
Downstream gene distance
SNP risk allelers11118844-A
SNPsrs11118844
Merged
SNP id current11118844
Contextintron_variant
Intergenic0
Allele frequency0.855
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta1.46
%95 Ci[NR]
PlatformAffymetrix, Illumina [up to 2543887] (imputed)
CNVN
Mapped traitwhite matter lesion progression measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007746
Study accessionGCST003151