rs16879552
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs16879552(C;T) |
| Make rs16879552(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 32553698 |
| Gene | NRG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16879552 |
| dbSNP (classic) | rs16879552 |
| ClinGen | rs16879552 |
| ebi | rs16879552 |
| HLI | rs16879552 |
| Exac | rs16879552 |
| Gnomad | rs16879552 |
| Varsome | rs16879552 |
| LitVar | rs16879552 |
| Map | rs16879552 |
| PheGenI | rs16879552 |
| Biobank | rs16879552 |
| 1000 genomes | rs16879552 |
| hgdp | rs16879552 |
| ensembl | rs16879552 |
| geneview | rs16879552 |
| scholar | rs16879552 |
| rs16879552 | |
| pharmgkb | rs16879552 |
| gwascentral | rs16879552 |
| openSNP | rs16879552 |
| 23andMe | rs16879552 |
| SNPshot | rs16879552 |
| SNPdbe | rs16879552 |
| MSV3d | rs16879552 |
| GWAS Ctlg | rs16879552 |
| GMAF | 0.2433 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19196962
] Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
[PMID 21283760] Fine mapping of the NRG1 Hirschsprung's disease locus.
[PMID 25475805] Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease
[PMID 28256518] Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.
[PMID 32418639] Common variants of NRG1 and ITGB4 confer risk of Hirschsprung disease in Han Chinese population.
