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rs62507334

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Carrier of a phenylketonuria mutation
Make rs62507334(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843793
GenePAH
is asnp
is mentioned by
dbSNPrs62507334
ebirs62507334
HLIrs62507334
Exacrs62507334
Varsomers62507334
Maprs62507334
PheGenIrs62507334
hapmaprs62507334
1000 genomesrs62507334
hgdprs62507334
ensemblrs62507334
gopubmedrs62507334
geneviewrs62507334
scholarrs62507334
googlers62507334
pharmgkbrs62507334
gwascentralrs62507334
openSNPrs62507334
23andMers62507334
23andMe allrs62507334
SNP Nexus

SNPshotrs62507334
SNPdbers62507334
MSV3drs62507334
GWAS Ctlgrs62507334
Max Magnitude3
ClinVar
Risk rs62507334(G,T;G,T)
Alt rs62507334(G,T;G,T)
Reference rs62507334(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237571G>C
CLNSRC
CLNACC RCV000088739.1,