rs3817446
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3817446(A;A) |
Make rs3817446(A;G) |
Make rs3817446(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 102867041 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs3817446 |
dbSNP (classic) | rs3817446 |
ClinGen | rs3817446 |
ebi | rs3817446 |
HLI | rs3817446 |
Exac | rs3817446 |
Gnomad | rs3817446 |
Varsome | rs3817446 |
LitVar | rs3817446 |
Map | rs3817446 |
PheGenI | rs3817446 |
Biobank | rs3817446 |
1000 genomes | rs3817446 |
hgdp | rs3817446 |
ensembl | rs3817446 |
geneview | rs3817446 |
scholar | rs3817446 |
rs3817446 | |
pharmgkb | rs3817446 |
gwascentral | rs3817446 |
openSNP | rs3817446 |
23andMe | rs3817446 |
SNPshot | rs3817446 |
SNPdbe | rs3817446 |
MSV3d | rs3817446 |
GWAS Ctlg | rs3817446 |
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