rs6140226
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6140226(C;C) |
| Make rs6140226(C;T) |
| Make rs6140226(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 7245836 |
| Gene | LINC01428 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6140226 |
| dbSNP (classic) | rs6140226 |
| ClinGen | rs6140226 |
| ebi | rs6140226 |
| HLI | rs6140226 |
| Exac | rs6140226 |
| Gnomad | rs6140226 |
| Varsome | rs6140226 |
| LitVar | rs6140226 |
| Map | rs6140226 |
| PheGenI | rs6140226 |
| Biobank | rs6140226 |
| 1000 genomes | rs6140226 |
| hgdp | rs6140226 |
| ensembl | rs6140226 |
| geneview | rs6140226 |
| scholar | rs6140226 |
| rs6140226 | |
| pharmgkb | rs6140226 |
| gwascentral | rs6140226 |
| openSNP | rs6140226 |
| 23andMe | rs6140226 |
| SNPshot | rs6140226 |
| SNPdbe | rs6140226 |
| MSV3d | rs6140226 |
| GWAS Ctlg | rs6140226 |
| GMAF | 0.4238 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 23160099
] A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
[PMID 17186469] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
