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rs281865453

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281865453(A;G)
Make rs281865453(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position102843674
GenePAH
is asnp
is mentioned by
dbSNPrs281865453
ebirs281865453
HLIrs281865453
Exacrs281865453
Varsomers281865453
Maprs281865453
PheGenIrs281865453
hapmaprs281865453
1000 genomesrs281865453
hgdprs281865453
ensemblrs281865453
gopubmedrs281865453
geneviewrs281865453
scholarrs281865453
googlers281865453
pharmgkbrs281865453
gwascentralrs281865453
openSNPrs281865453
23andMers281865453
23andMe allrs281865453
SNP Nexus

SNPshotrs281865453
SNPdbers281865453
MSV3drs281865453
GWAS Ctlgrs281865453
Max Magnitude0
ClinVar
Risk rs281865453(G;G)
Alt rs281865453(G;G)
Reference rs281865453(A;A)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103237452T>C
CLNSRC ClinVar
CLNACC RCV000106342.1,