Difference between revisions of "Rs137853277"
From SNPedia
SNPediaBot (talk | contribs) m (added ClinVar data) |
m (Update Rsnum - Set: Chromosome Orientation geno1 geno2 geno3 Gene position Gene_s Assembly GenomeBuild dbSNPBuild) |
||
| Line 1: | Line 1: | ||
{{Rsnum | {{Rsnum | ||
|rsid=137853277 | |rsid=137853277 | ||
| − | }} | + | |Chromosome=1 |
| − | {{ClinVar | + | |Orientation=minus |
| + | |geno1=(C;C) | ||
| + | |geno2=(C;T) | ||
| + | |geno3=(T;T) | ||
| + | |Gene=MYOC | ||
| + | |position=171605522 | ||
| + | |Gene_s=MYOC | ||
| + | |Assembly=GRCh37.p5 | ||
| + | |GenomeBuild=37.3 | ||
| + | |dbSNPBuild=137 | ||
| + | }}{{ClinVar | ||
|rsid=137853277 | |rsid=137853277 | ||
|Reversed=1 | |Reversed=1 | ||
Revision as of 18:02, 30 July 2012
| Orientation | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs137853277(C;T) |
| Make rs137853277(T;T) |
| Reference | GRCh37.p5 37.3/137 |
| Chromosome | 1 |
| Position | 171605522 |
| Gene | MYOC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137853277 |
| dbSNP (classic) | rs137853277 |
| ClinGen | rs137853277 |
| ebi | rs137853277 |
| HLI | rs137853277 |
| Exac | rs137853277 |
| Gnomad | rs137853277 |
| Varsome | rs137853277 |
| LitVar | rs137853277 |
| Map | rs137853277 |
| PheGenI | rs137853277 |
| Biobank | rs137853277 |
| 1000 genomes | rs137853277 |
| hgdp | rs137853277 |
| ensembl | rs137853277 |
| geneview | rs137853277 |
| scholar | rs137853277 |
| rs137853277 | |
| pharmgkb | rs137853277 |
| gwascentral | rs137853277 |
| openSNP | rs137853277 |
| 23andMe | rs137853277 |
| SNPshot | rs137853277 |
| SNPdbe | rs137853277 |
| MSV3d | rs137853277 |
| GWAS Ctlg | rs137853277 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs137853277(T;T) |
| Alt | rs137853277(T;T) |
| Reference | Rs137853277(C;C) |
| Significance | Probable-Pathogenic |
| Disease | OMIM |
| Variation | info |
| Gene | MYOC |
| CLNDBN | OMIM |
| Reversed | 1 |
| HGVS | NC_000001.10:g.171605522G>A |
| CLNSRC | |
| CLNACC | |
