rs1718301
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1718301(A;A) |
| Make rs1718301(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 102877415 |
| Gene | PAH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1718301 |
| dbSNP (classic) | rs1718301 |
| ClinGen | rs1718301 |
| ebi | rs1718301 |
| HLI | rs1718301 |
| Exac | rs1718301 |
| Gnomad | rs1718301 |
| Varsome | rs1718301 |
| LitVar | rs1718301 |
| Map | rs1718301 |
| PheGenI | rs1718301 |
| Biobank | rs1718301 |
| 1000 genomes | rs1718301 |
| hgdp | rs1718301 |
| ensembl | rs1718301 |
| geneview | rs1718301 |
| scholar | rs1718301 |
| rs1718301 | |
| pharmgkb | rs1718301 |
| gwascentral | rs1718301 |
| openSNP | rs1718301 |
| 23andMe | rs1718301 |
| SNPshot | rs1718301 |
| SNPdbe | rs1718301 |
| MSV3d | rs1718301 |
| GWAS Ctlg | rs1718301 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23898865
] Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults
| ClinVar | |
|---|---|
| Risk | rs1718301(A;A) |
| Alt | rs1718301(A;A) |
| Reference | Rs1718301(G;G) |
| Significance | Non-pathogenic |
| Disease | not provided not specified |
| Variation | info |
| Gene | PAH |
| CLNDBN | not provided not specified |
| Reversed | 0 |
| HGVS | NC_000012.11:g.103271193G>A |
| CLNSRC | |
| CLNACC | RCV000088921.1, RCV000244724.1, |
