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rs62508674

From SNPedia

Orientationminus
Geno Mag Summary
(A;G) 3 Carrier of a phenylketonuria mutation
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a phenylketonuria mutation
Make rs62508674(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843641
GenePAH
is asnp
is mentioned by
dbSNPrs62508674
ebirs62508674
HLIrs62508674
Exacrs62508674
Varsomers62508674
Maprs62508674
PheGenIrs62508674
hapmaprs62508674
1000 genomesrs62508674
hgdprs62508674
ensemblrs62508674
gopubmedrs62508674
geneviewrs62508674
scholarrs62508674
googlers62508674
pharmgkbrs62508674
gwascentralrs62508674
openSNPrs62508674
23andMers62508674
23andMe allrs62508674
SNP Nexus

SNPshotrs62508674
SNPdbers62508674
MSV3drs62508674
GWAS Ctlgrs62508674
Max Magnitude3
ClinVar
Risk rs62508674(T;T)
Alt rs62508674(T;T)
Reference rs62508674(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237419C>A
CLNSRC
CLNACC RCV000088794.1,