rs1051246
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1051246(C;C) |
| Make rs1051246(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 79938062 |
| Gene | SFTPD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1051246 |
| dbSNP (classic) | rs1051246 |
| ClinGen | rs1051246 |
| ebi | rs1051246 |
| HLI | rs1051246 |
| Exac | rs1051246 |
| Gnomad | rs1051246 |
| Varsome | rs1051246 |
| LitVar | rs1051246 |
| Map | rs1051246 |
| PheGenI | rs1051246 |
| Biobank | rs1051246 |
| 1000 genomes | rs1051246 |
| hgdp | rs1051246 |
| ensembl | rs1051246 |
| geneview | rs1051246 |
| scholar | rs1051246 |
| rs1051246 | |
| pharmgkb | rs1051246 |
| gwascentral | rs1051246 |
| openSNP | rs1051246 |
| 23andMe | rs1051246 |
| SNPshot | rs1051246 |
| SNPdbe | rs1051246 |
| MSV3d | rs1051246 |
| GWAS Ctlg | rs1051246 |
| GMAF | 0.1469 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21857919
] Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM)
| ClinVar | |
|---|---|
| Risk | rs1051246(C;C) |
| Alt | rs1051246(C;C) |
| Reference | Rs1051246(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | SFTPD |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000010.10:g.81697818A>G |
| CLNSRC | |
| CLNACC | RCV000155579.1, |
