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rs62507261

From SNPedia

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


Make rs62507261(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102840523
GenePAH
is asnp
is mentioned by
dbSNPrs62507261
ebirs62507261
HLIrs62507261
Exacrs62507261
Varsomers62507261
Maprs62507261
PheGenIrs62507261
hapmaprs62507261
1000 genomesrs62507261
hgdprs62507261
ensemblrs62507261
gopubmedrs62507261
geneviewrs62507261
scholarrs62507261
googlers62507261
pharmgkbrs62507261
gwascentralrs62507261
openSNPrs62507261
23andMers62507261
23andMe allrs62507261
SNP Nexus

SNPshotrs62507261
SNPdbers62507261
MSV3drs62507261
GWAS Ctlgrs62507261
Max Magnitude3
ClinVar
Risk rs62507261(A,C,T;A,C,T)
Alt rs62507261(A,C,T;A,C,T)
Reference rs62507261(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103234301C>T
CLNSRC
CLNACC RCV000088799.1,