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rs62517199

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 Carrier of a phenylketonuria mutation
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs62517199(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844433
GenePAH
is asnp
is mentioned by
dbSNPrs62517199
ebirs62517199
HLIrs62517199
Exacrs62517199
Varsomers62517199
Maprs62517199
PheGenIrs62517199
hapmaprs62517199
1000 genomesrs62517199
hgdprs62517199
ensemblrs62517199
gopubmedrs62517199
geneviewrs62517199
scholarrs62517199
googlers62517199
pharmgkbrs62517199
gwascentralrs62517199
openSNPrs62517199
23andMers62517199
23andMe allrs62517199
SNP Nexus

SNPshotrs62517199
SNPdbers62517199
MSV3drs62517199
GWAS Ctlgrs62517199
Max Magnitude3
ClinVar
Risk rs62517199(C;C)
Alt rs62517199(C;C)
Reference rs62517199(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238211T>G
CLNSRC
CLNACC RCV000089184.1,