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rs62514902

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62514902(G;T)
Make rs62514902(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102894837
GenePAH
is asnp
is mentioned by
dbSNPrs62514902
ebirs62514902
HLIrs62514902
Exacrs62514902
Varsomers62514902
Maprs62514902
PheGenIrs62514902
hapmaprs62514902
1000 genomesrs62514902
hgdprs62514902
ensemblrs62514902
gopubmedrs62514902
geneviewrs62514902
scholarrs62514902
googlers62514902
pharmgkbrs62514902
gwascentralrs62514902
openSNPrs62514902
23andMers62514902
23andMe allrs62514902
SNP Nexus

SNPshotrs62514902
SNPdbers62514902
MSV3drs62514902
GWAS Ctlgrs62514902
Max Magnitude0
ClinVar
Risk rs62514902(T;T)
Alt rs62514902(T;T)
Reference rs62514902(G;G)
Significance Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103288615C>A
CLNSRC
CLNACC RCV000088883.1, RCV000177027.1,