Have questions? Visit https://www.reddit.com/r/SNPedia

rs796064504

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796064504(C;C)
Make rs796064504(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102851704
GenePAH
is asnp
is mentioned by
dbSNPrs796064504
ebirs796064504
HLIrs796064504
Exacrs796064504
Varsomers796064504
Maprs796064504
PheGenIrs796064504
hapmaprs796064504
1000 genomesrs796064504
hgdprs796064504
ensemblrs796064504
gopubmedrs796064504
geneviewrs796064504
scholarrs796064504
googlers796064504
pharmgkbrs796064504
gwascentralrs796064504
openSNPrs796064504
23andMers796064504
23andMe allrs796064504
SNP Nexus

SNPshotrs796064504
SNPdbers796064504
MSV3drs796064504
GWAS Ctlgrs796064504
Max Magnitude0
ClinVar
Risk rs796064504(C;C)
Alt rs796064504(C;C)
Reference rs796064504(T;T)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103245482A>G
CLNSRC
CLNACC RCV000190378.1,