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rs62508737

From SNPedia

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


Make rs62508737(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843644
GenePAH
is asnp
is mentioned by
dbSNPrs62508737
ebirs62508737
HLIrs62508737
Exacrs62508737
Varsomers62508737
Maprs62508737
PheGenIrs62508737
hapmaprs62508737
1000 genomesrs62508737
hgdprs62508737
ensemblrs62508737
gopubmedrs62508737
geneviewrs62508737
scholarrs62508737
googlers62508737
pharmgkbrs62508737
gwascentralrs62508737
openSNPrs62508737
23andMers62508737
23andMe allrs62508737
SNP Nexus

SNPshotrs62508737
SNPdbers62508737
MSV3drs62508737
GWAS Ctlgrs62508737
Max Magnitude3
ClinVar
Risk rs62508737(C;C)
Alt rs62508737(C;C)
Reference rs62508737(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237422A>G
CLNSRC
CLNACC RCV000088793.1,