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rs796064502

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796064502(A;A)
Make rs796064502(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102894845
GenePAH
is asnp
is mentioned by
dbSNPrs796064502
ebirs796064502
HLIrs796064502
Exacrs796064502
Varsomers796064502
Maprs796064502
PheGenIrs796064502
hapmaprs796064502
1000 genomesrs796064502
hgdprs796064502
ensemblrs796064502
gopubmedrs796064502
geneviewrs796064502
scholarrs796064502
googlers796064502
pharmgkbrs796064502
gwascentralrs796064502
openSNPrs796064502
23andMers796064502
23andMe allrs796064502
SNP Nexus

SNPshotrs796064502
SNPdbers796064502
MSV3drs796064502
GWAS Ctlgrs796064502
Max Magnitude0
ClinVar
Risk rs796064502(A;A)
Alt rs796064502(A;A)
Reference rs796064502(C;C)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103288623G>T
CLNSRC
CLNACC RCV000190376.1,