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rs62507335

From SNPedia

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


Make rs62507335(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852863
GenePAH
is asnp
is mentioned by
dbSNPrs62507335
ebirs62507335
HLIrs62507335
Exacrs62507335
Varsomers62507335
Maprs62507335
PheGenIrs62507335
hapmaprs62507335
1000 genomesrs62507335
hgdprs62507335
ensemblrs62507335
gopubmedrs62507335
geneviewrs62507335
scholarrs62507335
googlers62507335
pharmgkbrs62507335
gwascentralrs62507335
openSNPrs62507335
23andMers62507335
23andMe allrs62507335
SNP Nexus

SNPshotrs62507335
SNPdbers62507335
MSV3drs62507335
GWAS Ctlgrs62507335
Max Magnitude3
ClinVar
Risk rs62507335(A;A)
Alt rs62507335(A;A)
Reference rs62507335(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246641C>T
CLNSRC
CLNACC RCV000089095.1,