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rs5030842

From SNPedia

Orientationminus
Geno Mag Summary
(C;T) 3 Carrier of a phenylketonuria mutation
(T;T) 0 common in clinvar


Make rs5030842(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102894888
GenePAH
is asnp
is mentioned by
dbSNPrs5030842
ebirs5030842
HLIrs5030842
Exacrs5030842
Varsomers5030842
Maprs5030842
PheGenIrs5030842
hapmaprs5030842
1000 genomesrs5030842
hgdprs5030842
ensemblrs5030842
gopubmedrs5030842
geneviewrs5030842
scholarrs5030842
googlers5030842
pharmgkbrs5030842
gwascentralrs5030842
openSNPrs5030842
23andMers5030842
23andMe allrs5030842
SNP Nexus

SNPshotrs5030842
SNPdbers5030842
MSV3drs5030842
GWAS Ctlgrs5030842
Max Magnitude3
ClinVar
Risk rs5030842(C;C)
Alt rs5030842(C;C)
Reference rs5030842(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103288666A>G
CLNSRC
CLNACC RCV000088867.1,