rs35910969
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs35910969(C;G) |
| Make rs35910969(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 74749174 |
| Gene | LOC105371893, MIR3615, SLC9A3R1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35910969 |
| dbSNP (classic) | rs35910969 |
| ClinGen | rs35910969 |
| ebi | rs35910969 |
| HLI | rs35910969 |
| Exac | rs35910969 |
| Gnomad | rs35910969 |
| Varsome | rs35910969 |
| LitVar | rs35910969 |
| Map | rs35910969 |
| PheGenI | rs35910969 |
| Biobank | rs35910969 |
| 1000 genomes | rs35910969 |
| hgdp | rs35910969 |
| ensembl | rs35910969 |
| geneview | rs35910969 |
| scholar | rs35910969 |
| rs35910969 | |
| pharmgkb | rs35910969 |
| gwascentral | rs35910969 |
| openSNP | rs35910969 |
| 23andMe | rs35910969 |
| SNPshot | rs35910969 |
| SNPdbe | rs35910969 |
| MSV3d | rs35910969 |
| GWAS Ctlg | rs35910969 |
| GMAF | 0.01194 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs35910969(G;G) |
| Alt | rs35910969(G;G) |
| Reference | Rs35910969(C;C) |
| Significance | Pathogenic |
| Disease | Nephrolithiasis/osteoporosis |
| Variation | info |
| Gene | MIR3615 SLC9A3R1 |
| CLNDBN | Nephrolithiasis/osteoporosis, hypophosphatemic, 2 |
| Reversed | 0 |
| HGVS | NC_000017.10:g.72745313C>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000005588.2, |
