rs199475687
From SNPedia
| Merged into | rs62642094 |
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;CTT) | 3 | Carrier of a phenylketonuria mutation |
| (TCT;TCT) | 0 | common in clinvar |
| Make rs199475687(-;-) |
| Make rs199475687(CTT;CTT) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 12 |
| Position | 102894879 |
| Gene | PAH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199475687 |
| dbSNP (classic) | rs199475687 |
| ClinGen | rs199475687 |
| ebi | rs199475687 |
| HLI | rs199475687 |
| Exac | rs199475687 |
| Gnomad | rs199475687 |
| Varsome | rs199475687 |
| LitVar | rs199475687 |
| Map | rs199475687 |
| PheGenI | rs199475687 |
| Biobank | rs199475687 |
| 1000 genomes | rs199475687 |
| hgdp | rs199475687 |
| ensembl | rs199475687 |
| geneview | rs199475687 |
| scholar | rs199475687 |
| rs199475687 | |
| pharmgkb | rs199475687 |
| gwascentral | rs199475687 |
| openSNP | rs199475687 |
| 23andMe | rs199475687 |
| SNPshot | rs199475687 |
| SNPdbe | rs199475687 |
| MSV3d | rs199475687 |
| GWAS Ctlg | rs199475687 |
| Status | Merged into rs62642094 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs199475687(TCT;TCT) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | PAH |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000012.11:g.103288655_103288657delAGA |
| CLNSRC | |
| CLNACC | RCV000088875.2, |
