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rs62508739

From SNPedia

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


Make rs62508739(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102851743
GenePAH
is asnp
is mentioned by
dbSNPrs62508739
ebirs62508739
HLIrs62508739
Exacrs62508739
Varsomers62508739
Maprs62508739
PheGenIrs62508739
hapmaprs62508739
1000 genomesrs62508739
hgdprs62508739
ensemblrs62508739
gopubmedrs62508739
geneviewrs62508739
scholarrs62508739
googlers62508739
pharmgkbrs62508739
gwascentralrs62508739
openSNPrs62508739
23andMers62508739
23andMe allrs62508739
SNP Nexus

SNPshotrs62508739
SNPdbers62508739
MSV3drs62508739
GWAS Ctlgrs62508739
Max Magnitude3
ClinVar
Risk rs62508739(A;A)
Alt rs62508739(A;A)
Reference rs62508739(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103245521C>T
CLNSRC
CLNACC RCV000089141.1,