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rs2037639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2037639(A;A)
Make rs2037639(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position102877572
GenePAH
is asnp
is mentioned by
dbSNPrs2037639
ebirs2037639
HLIrs2037639
Exacrs2037639
Varsomers2037639
Maprs2037639
PheGenIrs2037639
hapmaprs2037639
1000 genomesrs2037639
hgdprs2037639
ensemblrs2037639
gopubmedrs2037639
geneviewrs2037639
scholarrs2037639
googlers2037639
pharmgkbrs2037639
gwascentralrs2037639
openSNPrs2037639
23andMers2037639
23andMe allrs2037639
SNP Nexus

SNPshotrs2037639
SNPdbers2037639
MSV3drs2037639
GWAS Ctlgrs2037639
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 rs2037639(A;A)
Alt rs2037639(A;A)
Reference rs2037639(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.103271350G>A
CLNSRC
CLNACC RCV000088901.1,