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rs281865451

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865451(C;G)
Make rs281865451(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position102846954
GenePAH
is asnp
is mentioned by
dbSNPrs281865451
ebirs281865451
HLIrs281865451
Exacrs281865451
Varsomers281865451
Maprs281865451
PheGenIrs281865451
hapmaprs281865451
1000 genomesrs281865451
hgdprs281865451
ensemblrs281865451
gopubmedrs281865451
geneviewrs281865451
scholarrs281865451
googlers281865451
pharmgkbrs281865451
gwascentralrs281865451
openSNPrs281865451
23andMers281865451
23andMe allrs281865451
SNP Nexus

SNPshotrs281865451
SNPdbers281865451
MSV3drs281865451
GWAS Ctlgrs281865451
Max Magnitude0
ClinVar
Risk rs281865451(G;G)
Alt rs281865451(G;G)
Reference rs281865451(C;C)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103240732G>C
CLNSRC ClinVar
CLNACC RCV000106375.1,