rs797821
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs797821(A;G) |
| Make rs797821(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 83961536 |
| Gene | SEMA3A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs797821 |
| dbSNP (classic) | rs797821 |
| ClinGen | rs797821 |
| ebi | rs797821 |
| HLI | rs797821 |
| Exac | rs797821 |
| Gnomad | rs797821 |
| Varsome | rs797821 |
| LitVar | rs797821 |
| Map | rs797821 |
| PheGenI | rs797821 |
| Biobank | rs797821 |
| 1000 genomes | rs797821 |
| hgdp | rs797821 |
| ensembl | rs797821 |
| geneview | rs797821 |
| scholar | rs797821 |
| rs797821 | |
| pharmgkb | rs797821 |
| gwascentral | rs797821 |
| openSNP | rs797821 |
| 23andMe | rs797821 |
| SNPshot | rs797821 |
| SNPdbe | rs797821 |
| MSV3d | rs797821 |
| GWAS Ctlg | rs797821 |
| GMAF | 0.3779 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22184102] SEMA3A rs7804122 polymorphism is associated with Hirschsprung disease in the Northeastern region of China
| ClinVar | |
|---|---|
| Risk | rs797821(G;G) |
| Alt | rs797821(G;G) |
| Reference | Rs797821(A;A) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | SEMA3A |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000007.13:g.83590852T>C |
| CLNSRC | |
| CLNACC | RCV000175195.1, |
