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rs281865445

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281865445(G;G)
Make rs281865445(G;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position102852872
GenePAH
is asnp
is mentioned by
dbSNPrs281865445
ebirs281865445
HLIrs281865445
Exacrs281865445
Varsomers281865445
Maprs281865445
PheGenIrs281865445
hapmaprs281865445
1000 genomesrs281865445
hgdprs281865445
ensemblrs281865445
gopubmedrs281865445
geneviewrs281865445
scholarrs281865445
googlers281865445
pharmgkbrs281865445
gwascentralrs281865445
openSNPrs281865445
23andMers281865445
23andMe allrs281865445
SNP Nexus

SNPshotrs281865445
SNPdbers281865445
MSV3drs281865445
GWAS Ctlgrs281865445
Max Magnitude0
ClinVar
Risk rs281865445(G;G)
Alt rs281865445(G;G)
Reference rs281865445(T;T)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103246650A>C
CLNSRC ClinVar
CLNACC RCV000106366.1,