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rs62507279

From SNPedia

Orientationminus
Geno Mag Summary
(A;C) 3 Carrier of a phenylketonuria mutation
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a phenylketonuria mutation
Make rs62507279(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844355
GenePAH
is asnp
is mentioned by
dbSNPrs62507279
ebirs62507279
HLIrs62507279
Exacrs62507279
Varsomers62507279
Maprs62507279
PheGenIrs62507279
hapmaprs62507279
1000 genomesrs62507279
hgdprs62507279
ensemblrs62507279
gopubmedrs62507279
geneviewrs62507279
scholarrs62507279
googlers62507279
pharmgkbrs62507279
gwascentralrs62507279
openSNPrs62507279
23andMers62507279
23andMe allrs62507279
SNP Nexus

SNPshotrs62507279
SNPdbers62507279
MSV3drs62507279
GWAS Ctlgrs62507279
Max Magnitude3
ClinVar
Risk rs62507279(A,T;A,T)
Alt rs62507279(A,T;A,T)
Reference rs62507279(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238133G>A; NC_000012.11:g.103238133G>T
CLNSRC
CLNACC RCV000088723.1, RCV000088722.1,