rs606231208
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (CTGCAGCTG;CTGCAGCTG) | 0 | common in clinvar | 
| Make rs606231208(-;-) | 
| Make rs606231208(-;CTGCAGCTG) | 
| Reference | GRCh38.p2 38.2/144 | 
| Chromosome | 9 | 
| Position | 124500261 | 
| Gene | NR5A1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs606231208 | 
| dbSNP (classic) | rs606231208 | 
| ClinGen | rs606231208 | 
| ebi | rs606231208 | 
| HLI | rs606231208 | 
| Exac | rs606231208 | 
| Gnomad | rs606231208 | 
| Varsome | rs606231208 | 
| LitVar | rs606231208 | 
| Map | rs606231208 | 
| PheGenI | rs606231208 | 
| Biobank | rs606231208 | 
| 1000 genomes | rs606231208 | 
| hgdp | rs606231208 | 
| ensembl | rs606231208 | 
| geneview | rs606231208 | 
| scholar | rs606231208 | 
| rs606231208 | |
| pharmgkb | rs606231208 | 
| gwascentral | rs606231208 | 
| openSNP | rs606231208 | 
| 23andMe | rs606231208 | 
| SNPshot | rs606231208 | 
| SNPdbe | rs606231208 | 
| MSV3d | rs606231208 | 
| GWAS Ctlg | rs606231208 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs606231208(-;-) | 
| Alt | rs606231208(-;-) | 
| Reference | Rs606231208(CTGCAGCTG;CTGCAGCTG) | 
| Significance | Pathogenic | 
| Disease | Premature ovarian failure 7 | 
| Variation | info | 
| Gene | NR5A1 | 
| CLNDBN | Premature ovarian failure 7 | 
| Reversed | 1 | 
| HGVS | NC_000009.11:g.127262540_127262548delCAGCTGCAG | 
| CLNSRC | OMIM Allelic Variant | 
| CLNACC | RCV000013656.18, | 


