rs797044452
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs797044452(A;A) |
| Make rs797044452(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 67744788 |
| Gene | GNRHR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs797044452 |
| dbSNP (classic) | rs797044452 |
| ClinGen | rs797044452 |
| ebi | rs797044452 |
| HLI | rs797044452 |
| Exac | rs797044452 |
| Gnomad | rs797044452 |
| Varsome | rs797044452 |
| LitVar | rs797044452 |
| Map | rs797044452 |
| PheGenI | rs797044452 |
| Biobank | rs797044452 |
| 1000 genomes | rs797044452 |
| hgdp | rs797044452 |
| ensembl | rs797044452 |
| geneview | rs797044452 |
| scholar | rs797044452 |
| rs797044452 | |
| pharmgkb | rs797044452 |
| gwascentral | rs797044452 |
| openSNP | rs797044452 |
| 23andMe | rs797044452 |
| SNPshot | rs797044452 |
| SNPdbe | rs797044452 |
| MSV3d | rs797044452 |
| GWAS Ctlg | rs797044452 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs797044452(A;A) |
| Alt | rs797044452(A;A) |
| Reference | Rs797044452(G;G) |
| Significance | Pathogenic |
| Disease | Hypogonadotropic hypogonadism 7 with or without anosmia |
| Variation | info |
| Gene | GNRHR |
| CLNDBN | Hypogonadotropic hypogonadism 7 with or without anosmia |
| Reversed | 1 |
| HGVS | NC_000004.11:g.68610506C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000030917.29, |
