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rs62644503

From SNPedia

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


Make rs62644503(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102852902
GenePAH
is asnp
is mentioned by
dbSNPrs62644503
ebirs62644503
HLIrs62644503
Exacrs62644503
Varsomers62644503
Maprs62644503
PheGenIrs62644503
hapmaprs62644503
1000 genomesrs62644503
hgdprs62644503
ensemblrs62644503
gopubmedrs62644503
geneviewrs62644503
scholarrs62644503
googlers62644503
pharmgkbrs62644503
gwascentralrs62644503
openSNPrs62644503
23andMers62644503
23andMe allrs62644503
SNP Nexus

SNPshotrs62644503
SNPdbers62644503
MSV3drs62644503
GWAS Ctlgrs62644503
Max Magnitude3
ClinVar
Risk rs62644503(A;A)
Alt rs62644503(A;A)
Reference rs62644503(G;G)
Significance Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103246680C>T
CLNSRC
CLNACC RCV000089080.1, RCV000179742.1,