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rs62509018

From SNPedia

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


Make rs62509018(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843626
GenePAH
is asnp
is mentioned by
dbSNPrs62509018
dbSNP (old)rs62509018
ClinGenrs62509018
ebirs62509018
HLIrs62509018
Exacrs62509018
Varsomers62509018
Maprs62509018
PheGenIrs62509018
Biobankrs62509018
1000 genomesrs62509018
hgdprs62509018
ensemblrs62509018
gopubmedrs62509018
geneviewrs62509018
scholarrs62509018
googlers62509018
pharmgkbrs62509018
gwascentralrs62509018
openSNPrs62509018
23andMers62509018
23andMe allrs62509018
SNP Nexus

SNPshotrs62509018
SNPdbers62509018
MSV3drs62509018
GWAS Ctlgrs62509018
Max Magnitude3
ClinVar
Risk rs62509018(C;C)
Alt rs62509018(C;C)
Reference Rs62509018(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237404C>G
CLNSRC
CLNACC RCV000088792.1,