rs1722387
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1722387(A;A) |
Make rs1722387(A;G) |
Make rs1722387(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 102847292 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs1722387 |
dbSNP (classic) | rs1722387 |
ClinGen | rs1722387 |
ebi | rs1722387 |
HLI | rs1722387 |
Exac | rs1722387 |
Gnomad | rs1722387 |
Varsome | rs1722387 |
LitVar | rs1722387 |
Map | rs1722387 |
PheGenI | rs1722387 |
Biobank | rs1722387 |
1000 genomes | rs1722387 |
hgdp | rs1722387 |
ensembl | rs1722387 |
geneview | rs1722387 |
scholar | rs1722387 |
rs1722387 | |
pharmgkb | rs1722387 |
gwascentral | rs1722387 |
openSNP | rs1722387 |
23andMe | rs1722387 |
SNPshot | rs1722387 |
SNPdbe | rs1722387 |
MSV3d | rs1722387 |
GWAS Ctlg | rs1722387 |
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