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rs62508589

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a phenylketonuria mutation
Make rs62508589(A;A)
Make rs62508589(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844406
GenePAH
is asnp
is mentioned by
dbSNPrs62508589
ebirs62508589
HLIrs62508589
Exacrs62508589
Varsomers62508589
Maprs62508589
PheGenIrs62508589
hapmaprs62508589
1000 genomesrs62508589
hgdprs62508589
ensemblrs62508589
gopubmedrs62508589
geneviewrs62508589
scholarrs62508589
googlers62508589
pharmgkbrs62508589
gwascentralrs62508589
openSNPrs62508589
23andMers62508589
23andMe allrs62508589
SNP Nexus

SNPshotrs62508589
SNPdbers62508589
MSV3drs62508589
GWAS Ctlgrs62508589
Max Magnitude3
ClinVar
Risk rs62508589(A;A)
Alt rs62508589(A;A)
Reference rs62508589(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238184C>T
CLNSRC
CLNACC RCV000089194.1,