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rs863225301

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225301(G;T)
Make rs863225301(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102878057
GenePAH
is asnp
is mentioned by
dbSNPrs863225301
ebirs863225301
HLIrs863225301
Exacrs863225301
Varsomers863225301
Maprs863225301
PheGenIrs863225301
hapmaprs863225301
1000 genomesrs863225301
hgdprs863225301
ensemblrs863225301
gopubmedrs863225301
geneviewrs863225301
scholarrs863225301
googlers863225301
pharmgkbrs863225301
gwascentralrs863225301
openSNPrs863225301
23andMers863225301
23andMe allrs863225301
SNP Nexus

SNPshotrs863225301
SNPdbers863225301
MSV3drs863225301
GWAS Ctlgrs863225301
Max Magnitude0
ClinVar
Risk rs863225301(T;T)
Alt rs863225301(T;T)
Reference rs863225301(G;G)
Significance Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103271835C>A
CLNSRC
CLNACC RCV000201954.1,