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rs62517166

From SNPedia

Orientationminus
Geno Mag Summary
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs62517166(A;A)
Make rs62517166(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102877461
GenePAH
is asnp
is mentioned by
dbSNPrs62517166
ebirs62517166
HLIrs62517166
Exacrs62517166
Varsomers62517166
Maprs62517166
PheGenIrs62517166
hapmaprs62517166
1000 genomesrs62517166
hgdprs62517166
ensemblrs62517166
gopubmedrs62517166
geneviewrs62517166
scholarrs62517166
googlers62517166
pharmgkbrs62517166
gwascentralrs62517166
openSNPrs62517166
23andMers62517166
23andMe allrs62517166
SNP Nexus

SNPshotrs62517166
SNPdbers62517166
MSV3drs62517166
GWAS Ctlgrs62517166
Max Magnitude3
ClinVar
Risk rs62517166(A,C;A,C)
Alt rs62517166(A,C;A,C)
Reference rs62517166(G;G)
Significance Other
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103271239C>T
CLNSRC
CLNACC RCV000088919.1, RCV000169579.2,