Have questions? Visit https://www.reddit.com/r/SNPedia

rs281865437

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281865437(C;C)
Make rs281865437(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position102840475
GenePAH
is asnp
is mentioned by
dbSNPrs281865437
ebirs281865437
HLIrs281865437
Exacrs281865437
Varsomers281865437
Maprs281865437
PheGenIrs281865437
hapmaprs281865437
1000 genomesrs281865437
hgdprs281865437
ensemblrs281865437
gopubmedrs281865437
geneviewrs281865437
scholarrs281865437
googlers281865437
pharmgkbrs281865437
gwascentralrs281865437
openSNPrs281865437
23andMers281865437
23andMe allrs281865437
SNP Nexus

SNPshotrs281865437
SNPdbers281865437
MSV3drs281865437
GWAS Ctlgrs281865437
Max Magnitude0
ClinVar
Risk rs281865437(C;C)
Alt rs281865437(C;C)
Reference rs281865437(T;T)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103234253A>G
CLNSRC ClinVar
CLNACC RCV000106346.1,