rs142835989
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs142835989(G;T) |
| Make rs142835989(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 9 |
| Position | 37436750 |
| Gene | GRHPR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142835989 |
| dbSNP (classic) | rs142835989 |
| ClinGen | rs142835989 |
| ebi | rs142835989 |
| HLI | rs142835989 |
| Exac | rs142835989 |
| Gnomad | rs142835989 |
| Varsome | rs142835989 |
| LitVar | rs142835989 |
| Map | rs142835989 |
| PheGenI | rs142835989 |
| Biobank | rs142835989 |
| 1000 genomes | rs142835989 |
| hgdp | rs142835989 |
| ensembl | rs142835989 |
| geneview | rs142835989 |
| scholar | rs142835989 |
| rs142835989 | |
| pharmgkb | rs142835989 |
| gwascentral | rs142835989 |
| openSNP | rs142835989 |
| 23andMe | rs142835989 |
| SNPshot | rs142835989 |
| SNPdbe | rs142835989 |
| MSV3d | rs142835989 |
| GWAS Ctlg | rs142835989 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs142835989(T;T) |
| Alt | rs142835989(T;T) |
| Reference | Rs142835989(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GRHPR |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.37436747G>T |
| CLNSRC | |
| CLNACC | RCV000490104.1, |
