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rs1718301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1718301(A;A)
Make rs1718301(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position102877415
GenePAH
is asnp
is mentioned by
dbSNPrs1718301
ebirs1718301
HLIrs1718301
Exacrs1718301
Varsomers1718301
Maprs1718301
PheGenIrs1718301
hapmaprs1718301
1000 genomesrs1718301
hgdprs1718301
ensemblrs1718301
gopubmedrs1718301
geneviewrs1718301
scholarrs1718301
googlers1718301
pharmgkbrs1718301
gwascentralrs1718301
openSNPrs1718301
23andMers1718301
23andMe allrs1718301
SNP Nexus

SNPshotrs1718301
SNPdbers1718301
MSV3drs1718301
GWAS Ctlgrs1718301
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 23898865OA-icon.png] 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 Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.103271193G>A
CLNSRC
CLNACC RCV000088921.1,