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rs62644489

From SNPedia

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


Make rs62644489(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102840495
GenePAH
is asnp
is mentioned by
dbSNPrs62644489
ebirs62644489
HLIrs62644489
Exacrs62644489
Varsomers62644489
Maprs62644489
PheGenIrs62644489
hapmaprs62644489
1000 genomesrs62644489
hgdprs62644489
ensemblrs62644489
gopubmedrs62644489
geneviewrs62644489
scholarrs62644489
googlers62644489
pharmgkbrs62644489
gwascentralrs62644489
openSNPrs62644489
23andMers62644489
23andMe allrs62644489
SNP Nexus

SNPshotrs62644489
SNPdbers62644489
MSV3drs62644489
GWAS Ctlgrs62644489
Max Magnitude3
ClinVar
Risk rs62644489(;)
Alt rs62644489(;)
Reference rs62644489(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103234273delG
CLNSRC
CLNACC RCV000088805.1,