rs63186960
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;G) | 3 | Carrier of a phenylketonuria mutation |
| (G;G) | 0 | common in clinvar |
| Make rs63186960(-;-) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 12 |
| Position | 102840516 |
| Gene | PAH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs63186960 |
| dbSNP (classic) | rs63186960 |
| ClinGen | rs63186960 |
| ebi | rs63186960 |
| HLI | rs63186960 |
| Exac | rs63186960 |
| Gnomad | rs63186960 |
| Varsome | rs63186960 |
| LitVar | rs63186960 |
| Map | rs63186960 |
| PheGenI | rs63186960 |
| Biobank | rs63186960 |
| 1000 genomes | rs63186960 |
| hgdp | rs63186960 |
| ensembl | rs63186960 |
| geneview | rs63186960 |
| scholar | rs63186960 |
| rs63186960 | |
| pharmgkb | rs63186960 |
| gwascentral | rs63186960 |
| openSNP | rs63186960 |
| 23andMe | rs63186960 |
| SNPshot | rs63186960 |
| SNPdbe | rs63186960 |
| MSV3d | rs63186960 |
| GWAS Ctlg | rs63186960 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs63186960(-;-) |
| Alt | rs63186960(-;-) |
| Reference | Rs63186960(G;G) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | PAH |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000012.11:g.103234294delC |
| CLNSRC | |
| CLNACC | RCV000088798.1, |
