rs137852663
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs137852663(C;G) |
| Make rs137852663(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 101771528 |
| Gene | FGF8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137852663 |
| ClinGen | rs137852663 |
| ebi | rs137852663 |
| HLI | rs137852663 |
| Exac | rs137852663 |
| Varsome | rs137852663 |
| Map | rs137852663 |
| PheGenI | rs137852663 |
| hapmap | rs137852663 |
| 1000 genomes | rs137852663 |
| hgdp | rs137852663 |
| ensembl | rs137852663 |
| gopubmed | rs137852663 |
| geneview | rs137852663 |
| scholar | rs137852663 |
| rs137852663 | |
| pharmgkb | rs137852663 |
| gwascentral | rs137852663 |
| openSNP | rs137852663 |
| 23andMe | rs137852663 |
| 23andMe all | rs137852663 |
| SNP Nexus | |
| SNPshot | rs137852663 |
| SNPdbe | rs137852663 |
| MSV3d | rs137852663 |
| GWAS Ctlg | rs137852663 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs137852663(G;G) |
| Alt | rs137852663(G;G) |
| Reference | Rs137852663(C;C) |
| Significance | Pathogenic |
| Disease | Kallmann syndrome 6 |
| Variation | info |
| Gene | FGF8 |
| CLNDBN | Kallmann syndrome 6 |
| Reversed | 1 |
| HGVS | NC_000010.10:g.103531285G>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000009695.2, |
