rs875989810
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs875989810(G;T) |
| Make rs875989810(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 10 |
| Position | 49528426 |
| Gene | ERCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs875989810 |
| dbSNP (classic) | rs875989810 |
| ClinGen | rs875989810 |
| ebi | rs875989810 |
| HLI | rs875989810 |
| Exac | rs875989810 |
| Gnomad | rs875989810 |
| Varsome | rs875989810 |
| LitVar | rs875989810 |
| Map | rs875989810 |
| PheGenI | rs875989810 |
| Biobank | rs875989810 |
| 1000 genomes | rs875989810 |
| hgdp | rs875989810 |
| ensembl | rs875989810 |
| geneview | rs875989810 |
| scholar | rs875989810 |
| rs875989810 | |
| pharmgkb | rs875989810 |
| gwascentral | rs875989810 |
| openSNP | rs875989810 |
| 23andMe | rs875989810 |
| SNPshot | rs875989810 |
| SNPdbe | rs875989810 |
| MSV3d | rs875989810 |
| GWAS Ctlg | rs875989810 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs875989810(T;T) |
| Alt | rs875989810(T;T) |
| Reference | Rs875989810(G;G) |
| Significance | Pathogenic |
| Disease | Premature ovarian failure 11 |
| Variation | info |
| Gene | ERCC6 |
| CLNDBN | Premature ovarian failure 11 |
| Reversed | 1 |
| HGVS | NC_000010.10:g.50736472C>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000211122.1, |
