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rs62507262

From SNPedia

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


Make rs62507262(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852824
GenePAH
is asnp
is mentioned by
dbSNPrs62507262
ebirs62507262
HLIrs62507262
Exacrs62507262
Varsomers62507262
Maprs62507262
PheGenIrs62507262
hapmaprs62507262
1000 genomesrs62507262
hgdprs62507262
ensemblrs62507262
gopubmedrs62507262
geneviewrs62507262
scholarrs62507262
googlers62507262
pharmgkbrs62507262
gwascentralrs62507262
openSNPrs62507262
23andMers62507262
23andMe allrs62507262
SNP Nexus

SNPshotrs62507262
SNPdbers62507262
MSV3drs62507262
GWAS Ctlgrs62507262
Max Magnitude3
ClinVar
Risk rs62507262(A,T;A,T)
Alt rs62507262(A,T;A,T)
Reference rs62507262(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246602G>A; NC_000012.11:g.103246602G>T
CLNSRC
CLNACC RCV000089124.1, RCV000089123.1,