rs7835688
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7835688(C;C) |
| Make rs7835688(C;G) |
| Make rs7835688(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 32553981 |
| Gene | NRG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7835688 |
| dbSNP (classic) | rs7835688 |
| ClinGen | rs7835688 |
| ebi | rs7835688 |
| HLI | rs7835688 |
| Exac | rs7835688 |
| Gnomad | rs7835688 |
| Varsome | rs7835688 |
| LitVar | rs7835688 |
| Map | rs7835688 |
| PheGenI | rs7835688 |
| Biobank | rs7835688 |
| 1000 genomes | rs7835688 |
| hgdp | rs7835688 |
| ensembl | rs7835688 |
| geneview | rs7835688 |
| scholar | rs7835688 |
| rs7835688 | |
| pharmgkb | rs7835688 |
| gwascentral | rs7835688 |
| openSNP | rs7835688 |
| 23andMe | rs7835688 |
| SNPshot | rs7835688 |
| SNPdbe | rs7835688 |
| MSV3d | rs7835688 |
| GWAS Ctlg | rs7835688 |
| GMAF | 0.3352 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 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.
