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rs62507273

From SNPedia

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


Make rs62507273(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844436
GenePAH
is asnp
is mentioned by
dbSNPrs62507273
ebirs62507273
HLIrs62507273
Exacrs62507273
Varsomers62507273
Maprs62507273
PheGenIrs62507273
hapmaprs62507273
1000 genomesrs62507273
hgdprs62507273
ensemblrs62507273
gopubmedrs62507273
geneviewrs62507273
scholarrs62507273
googlers62507273
pharmgkbrs62507273
gwascentralrs62507273
openSNPrs62507273
23andMers62507273
23andMe allrs62507273
SNP Nexus

SNPshotrs62507273
SNPdbers62507273
MSV3drs62507273
GWAS Ctlgrs62507273
Max Magnitude3
ClinVar
Risk rs62507273(A;A)
Alt rs62507273(A;A)
Reference rs62507273(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238214A>T
CLNSRC
CLNACC RCV000089185.1,