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rs62642944

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Carrier of a phenylketonuria mutation
Make rs62642944(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852868
GenePAH
is asnp
is mentioned by
dbSNPrs62642944
ebirs62642944
HLIrs62642944
Exacrs62642944
Varsomers62642944
Maprs62642944
PheGenIrs62642944
hapmaprs62642944
1000 genomesrs62642944
hgdprs62642944
ensemblrs62642944
gopubmedrs62642944
geneviewrs62642944
scholarrs62642944
googlers62642944
pharmgkbrs62642944
gwascentralrs62642944
openSNPrs62642944
23andMers62642944
23andMe allrs62642944
SNP Nexus

SNPshotrs62642944
SNPdbers62642944
MSV3drs62642944
GWAS Ctlgrs62642944
Max Magnitude3
ClinVar
Risk rs62642944(G;G)
Alt rs62642944(G;G)
Reference rs62642944(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246646G>C
CLNSRC
CLNACC RCV000089092.1,