Rs1077861

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Orientationminus
Make rs1077861(A;A)
Make rs1077861(A;T)
Make rs1077861(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position50725636
GeneNOD2
is asnp
is mentioned by
dbSNPrs1077861
Exacrs1077861
PheGenIrs1077861
nextbiors1077861
hapmaprs1077861
1000 genomesrs1077861
hgdprs1077861
ensemblrs1077861
gopubmedrs1077861
geneviewrs1077861
scholarrs1077861
googlers1077861
pharmgkbrs1077861
gwascentralrs1077861
openSNPrs1077861
23andMers1077861
23andMe allrs1077861
SNP Nexus

SNPshotrs1077861
SNPdbers1077861
MSV3drs1077861
GMAF0.3893
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 21943069] A NOD2 gene polymorphism is associated with the prevalence and severity of chronic obstructive pulmonary disease in a Japanese population

[PMID 12019468OA-icon.png] CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.

[PMID 12577202OA-icon.png] A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews.

[PMID 16008671] Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults.