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rs62642908

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 Carrier of a phenylketonuria mutation
Make rs62642908(A;A)
Make rs62642908(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852887
GenePAH
is asnp
is mentioned by
dbSNPrs62642908
ebirs62642908
HLIrs62642908
Exacrs62642908
Varsomers62642908
Maprs62642908
PheGenIrs62642908
hapmaprs62642908
1000 genomesrs62642908
hgdprs62642908
ensemblrs62642908
gopubmedrs62642908
geneviewrs62642908
scholarrs62642908
googlers62642908
pharmgkbrs62642908
gwascentralrs62642908
openSNPrs62642908
23andMers62642908
23andMe allrs62642908
SNP Nexus

SNPshotrs62642908
SNPdbers62642908
MSV3drs62642908
GWAS Ctlgrs62642908
Max Magnitude3
ClinVar
Risk rs62642908(A,T;A,T)
Alt rs62642908(A,T;A,T)
Reference rs62642908(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246665C>A; NC_000012.11:g.103246665C>T
CLNSRC
CLNACC RCV000089087.1, RCV000089086.1,