rs1077861
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1077861(A;A) |
| Make rs1077861(A;T) |
| Make rs1077861(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 50725636 |
| Gene | NOD2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1077861 |
| dbSNP (classic) | rs1077861 |
| ClinGen | rs1077861 |
| ebi | rs1077861 |
| HLI | rs1077861 |
| Exac | rs1077861 |
| Gnomad | rs1077861 |
| Varsome | rs1077861 |
| LitVar | rs1077861 |
| Map | rs1077861 |
| PheGenI | rs1077861 |
| Biobank | rs1077861 |
| 1000 genomes | rs1077861 |
| hgdp | rs1077861 |
| ensembl | rs1077861 |
| geneview | rs1077861 |
| scholar | rs1077861 |
| rs1077861 | |
| pharmgkb | rs1077861 |
| gwascentral | rs1077861 |
| openSNP | rs1077861 |
| 23andMe | rs1077861 |
| SNPshot | rs1077861 |
| SNPdbe | rs1077861 |
| MSV3d | rs1077861 |
| GWAS Ctlg | rs1077861 |
| GMAF | 0.3893 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
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[PMID 21943069] A NOD2 gene polymorphism is associated with the prevalence and severity of chronic obstructive pulmonary disease in a Japanese population
[PMID 12019468
] CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.
[PMID 12577202] 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.
