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rs62508592

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a phenylketonuria mutation
Make rs62508592(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855119
GenePAH
is asnp
is mentioned by
dbSNPrs62508592
ebirs62508592
HLIrs62508592
Exacrs62508592
Varsomers62508592
Maprs62508592
PheGenIrs62508592
hapmaprs62508592
1000 genomesrs62508592
hgdprs62508592
ensemblrs62508592
gopubmedrs62508592
geneviewrs62508592
scholarrs62508592
googlers62508592
pharmgkbrs62508592
gwascentralrs62508592
openSNPrs62508592
23andMers62508592
23andMe allrs62508592
SNP Nexus

SNPshotrs62508592
SNPdbers62508592
MSV3drs62508592
GWAS Ctlgrs62508592
Max Magnitude3
ClinVar
Risk rs62508592(T;T)
Alt rs62508592(T;T)
Reference rs62508592(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103248897C>A
CLNSRC
CLNACC RCV000089043.1,