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rs62508688

From SNPedia

Orientationminus
Geno Mag Summary
(A;G) 3 Carrier of a phenylketonuria mutation
(G;G) 0 common in clinvar
Make rs62508688(C;C)
Make rs62508688(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844365
GenePAH
is asnp
is mentioned by
dbSNPrs62508688
ebirs62508688
HLIrs62508688
Exacrs62508688
Varsomers62508688
Maprs62508688
PheGenIrs62508688
hapmaprs62508688
1000 genomesrs62508688
hgdprs62508688
ensemblrs62508688
gopubmedrs62508688
geneviewrs62508688
scholarrs62508688
googlers62508688
pharmgkbrs62508688
gwascentralrs62508688
openSNPrs62508688
23andMers62508688
23andMe allrs62508688
SNP Nexus

SNPshotrs62508688
SNPdbers62508688
MSV3drs62508688
GWAS Ctlgrs62508688
Max Magnitude3
ClinVar
Risk rs62508688(A,C;A,C)
Alt rs62508688(A,C;A,C)
Reference rs62508688(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238143C>G; NC_000012.11:g.103238143C>T
CLNSRC
CLNACC RCV000088717.1, RCV000088716.1,