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rs62516061

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a phenylketonuria mutation
Make rs62516061(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844395
GenePAH
is asnp
is mentioned by
dbSNPrs62516061
ebirs62516061
HLIrs62516061
Exacrs62516061
Varsomers62516061
Maprs62516061
PheGenIrs62516061
hapmaprs62516061
1000 genomesrs62516061
hgdprs62516061
ensemblrs62516061
gopubmedrs62516061
geneviewrs62516061
scholarrs62516061
googlers62516061
pharmgkbrs62516061
gwascentralrs62516061
openSNPrs62516061
23andMers62516061
23andMe allrs62516061
SNP Nexus

SNPshotrs62516061
SNPdbers62516061
MSV3drs62516061
GWAS Ctlgrs62516061
Max Magnitude3
ClinVar
Risk rs62516061(G,T;G,T)
Alt rs62516061(G,T;G,T)
Reference rs62516061(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238173G>A
CLNSRC
CLNACC RCV000088696.1,