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rs62507344

From SNPedia

Orientationminus
Geno Mag Summary
(C;T) 3 Carrier of a phenylketonuria mutation
Make rs62507344(C;C)
Make rs62507344(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843782
GenePAH
is asnp
is mentioned by
dbSNPrs62507344
ebirs62507344
HLIrs62507344
Exacrs62507344
Varsomers62507344
Maprs62507344
PheGenIrs62507344
hapmaprs62507344
1000 genomesrs62507344
hgdprs62507344
ensemblrs62507344
gopubmedrs62507344
geneviewrs62507344
scholarrs62507344
googlers62507344
pharmgkbrs62507344
gwascentralrs62507344
openSNPrs62507344
23andMers62507344
23andMe allrs62507344
SNP Nexus

SNPshotrs62507344
SNPdbers62507344
MSV3drs62507344
GWAS Ctlgrs62507344
Max Magnitude3
ClinVar
Risk rs62507344(T;T)
Alt rs62507344(T;T)
Reference rs62507344(C;C)
Significance Other
Disease Phenylketonuria not provided
Variation info
Gene PAH
CLNDBN Phenylketonuria not provided
Reversed 1
HGVS NC_000012.11:g.103237560G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000654.5, RCV000088742.1,