rs869025214
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs869025214(A;A) |
| Make rs869025214(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 9 |
| Position | 74788613 |
| Gene | TRPM6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs869025214 |
| dbSNP (classic) | rs869025214 |
| ClinGen | rs869025214 |
| ebi | rs869025214 |
| HLI | rs869025214 |
| Exac | rs869025214 |
| Gnomad | rs869025214 |
| Varsome | rs869025214 |
| LitVar | rs869025214 |
| Map | rs869025214 |
| PheGenI | rs869025214 |
| Biobank | rs869025214 |
| 1000 genomes | rs869025214 |
| hgdp | rs869025214 |
| ensembl | rs869025214 |
| geneview | rs869025214 |
| scholar | rs869025214 |
| rs869025214 | |
| pharmgkb | rs869025214 |
| gwascentral | rs869025214 |
| openSNP | rs869025214 |
| 23andMe | rs869025214 |
| SNPshot | rs869025214 |
| SNPdbe | rs869025214 |
| MSV3d | rs869025214 |
| GWAS Ctlg | rs869025214 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs869025214(A;A) |
| Alt | rs869025214(A;A) |
| Reference | Rs869025214(G;G) |
| Significance | Pathogenic |
| Disease | Hypomagnesemia 1 |
| Variation | info |
| Gene | TRPM6 |
| CLNDBN | Hypomagnesemia 1, intestinal |
| Reversed | 1 |
| HGVS | NC_000009.11:g.77403529C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000207483.2, |
