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rs796064503

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796064503(C;T)
Make rs796064503(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102852821
GenePAH
is asnp
is mentioned by
dbSNPrs796064503
ebirs796064503
HLIrs796064503
Exacrs796064503
Varsomers796064503
Maprs796064503
PheGenIrs796064503
hapmaprs796064503
1000 genomesrs796064503
hgdprs796064503
ensemblrs796064503
gopubmedrs796064503
geneviewrs796064503
scholarrs796064503
googlers796064503
pharmgkbrs796064503
gwascentralrs796064503
openSNPrs796064503
23andMers796064503
23andMe allrs796064503
SNP Nexus

SNPshotrs796064503
SNPdbers796064503
MSV3drs796064503
GWAS Ctlgrs796064503
Max Magnitude0
ClinVar
Risk rs796064503(T;T)
Alt rs796064503(T;T)
Reference rs796064503(C;C)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103246599G>A
CLNSRC
CLNACC RCV000190377.1,