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rs281865441

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865441(A;A)
Make rs281865441(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position102855274
GenePAH
is asnp
is mentioned by
dbSNPrs281865441
ebirs281865441
HLIrs281865441
Exacrs281865441
Varsomers281865441
Maprs281865441
PheGenIrs281865441
hapmaprs281865441
1000 genomesrs281865441
hgdprs281865441
ensemblrs281865441
gopubmedrs281865441
geneviewrs281865441
scholarrs281865441
googlers281865441
pharmgkbrs281865441
gwascentralrs281865441
openSNPrs281865441
23andMers281865441
23andMe allrs281865441
SNP Nexus

SNPshotrs281865441
SNPdbers281865441
MSV3drs281865441
GWAS Ctlgrs281865441
Max Magnitude0
ClinVar
Risk rs281865441(A;A)
Alt rs281865441(A;A)
Reference rs281865441(G;G)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103249052C>T
CLNSRC ClinVar
CLNACC RCV000106360.1,