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rs62516109

From SNPedia

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


Make rs62516109(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position102855204
GenePAH
is asnp
is mentioned by
dbSNPrs62516109
ebirs62516109
HLIrs62516109
Exacrs62516109
Varsomers62516109
Maprs62516109
PheGenIrs62516109
hapmaprs62516109
1000 genomesrs62516109
hgdprs62516109
ensemblrs62516109
gopubmedrs62516109
geneviewrs62516109
scholarrs62516109
googlers62516109
pharmgkbrs62516109
gwascentralrs62516109
openSNPrs62516109
23andMers62516109
23andMe allrs62516109
SNP Nexus

SNPshotrs62516109
SNPdbers62516109
MSV3drs62516109
GWAS Ctlgrs62516109
Max Magnitude3
ClinVar
Risk rs62516109(C;C)
Alt rs62516109(C;C)
Reference rs62516109(T;T)
Significance Other
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103248982A>G
CLNSRC HGMD
CLNACC RCV000078527.4, RCV000150086.5,