Difference between revisions of "Rs796052801"
From SNPedia
m (Update Rsnum - Set: Chromosome Orientation geno1 geno2 geno3 Gene position Gene_s Assembly GenomeBuild dbSNPBuild) |
OrientalBot (talk | contribs) (set StabilizedOrientation=minus) |
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|GenomeBuild=38.2 | |GenomeBuild=38.2 | ||
|dbSNPBuild=147 | |dbSNPBuild=147 | ||
| + | |StabilizedOrientation=minus | ||
}}{{ClinVar | }}{{ClinVar | ||
|ALT=C | |ALT=C | ||
Revision as of 01:57, 9 June 2017
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs796052801(C;G) |
| Make rs796052801(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | X |
| Position | 100408125 |
| Gene | PCDH19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs796052801 |
| dbSNP (classic) | rs796052801 |
| ClinGen | rs796052801 |
| ebi | rs796052801 |
| HLI | rs796052801 |
| Exac | rs796052801 |
| Gnomad | rs796052801 |
| Varsome | rs796052801 |
| LitVar | rs796052801 |
| Map | rs796052801 |
| PheGenI | rs796052801 |
| Biobank | rs796052801 |
| 1000 genomes | rs796052801 |
| hgdp | rs796052801 |
| ensembl | rs796052801 |
| geneview | rs796052801 |
| scholar | rs796052801 |
| rs796052801 | |
| pharmgkb | rs796052801 |
| gwascentral | rs796052801 |
| openSNP | rs796052801 |
| 23andMe | rs796052801 |
| SNPshot | rs796052801 |
| SNPdbe | rs796052801 |
| MSV3d | rs796052801 |
| GWAS Ctlg | rs796052801 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs796052801(G;G) |
| Alt | rs796052801(G;G) |
| Reference | Rs796052801(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PCDH19 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000023.10:g.99663123G>C |
| CLNSRC | |
| CLNACC | RCV000188351.1, |
