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rs62514951

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 3 Carrier of a phenylketonuria mutation
Make rs62514951(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852847
GenePAH
is asnp
is mentioned by
dbSNPrs62514951
ebirs62514951
HLIrs62514951
Exacrs62514951
Varsomers62514951
Maprs62514951
PheGenIrs62514951
hapmaprs62514951
1000 genomesrs62514951
hgdprs62514951
ensemblrs62514951
gopubmedrs62514951
geneviewrs62514951
scholarrs62514951
googlers62514951
pharmgkbrs62514951
gwascentralrs62514951
openSNPrs62514951
23andMers62514951
23andMe allrs62514951
SNP Nexus

SNPshotrs62514951
SNPdbers62514951
MSV3drs62514951
GWAS Ctlgrs62514951
Max Magnitude3
ClinVar
Risk rs62514951(T;T)
Alt rs62514951(T;T)
Reference rs62514951(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246625T>A
CLNSRC
CLNACC RCV000089106.1,