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rs281865435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281865435(C;C)
Make rs281865435(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position102843682
GenePAH
is asnp
is mentioned by
dbSNPrs281865435
ebirs281865435
HLIrs281865435
Exacrs281865435
Varsomers281865435
Maprs281865435
PheGenIrs281865435
hapmaprs281865435
1000 genomesrs281865435
hgdprs281865435
ensemblrs281865435
gopubmedrs281865435
geneviewrs281865435
scholarrs281865435
googlers281865435
pharmgkbrs281865435
gwascentralrs281865435
openSNPrs281865435
23andMers281865435
23andMe allrs281865435
SNP Nexus

SNPshotrs281865435
SNPdbers281865435
MSV3drs281865435
GWAS Ctlgrs281865435
Max Magnitude0
ClinVar
Risk rs281865435(C;C)
Alt rs281865435(C;C)
Reference rs281865435(T;T)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103237460A>G
CLNSRC ClinVar
CLNACC RCV000106341.1,