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rs62516141

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs62516141(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102843688
GenePAH
is asnp
is mentioned by
dbSNPrs62516141
ebirs62516141
HLIrs62516141
Exacrs62516141
Varsomers62516141
Maprs62516141
PheGenIrs62516141
hapmaprs62516141
1000 genomesrs62516141
hgdprs62516141
ensemblrs62516141
gopubmedrs62516141
geneviewrs62516141
scholarrs62516141
googlers62516141
pharmgkbrs62516141
gwascentralrs62516141
openSNPrs62516141
23andMers62516141
23andMe allrs62516141
SNP Nexus

SNPshotrs62516141
SNPdbers62516141
MSV3drs62516141
GWAS Ctlgrs62516141
Max Magnitude3
ClinVar
Risk rs62516141(G;G)
Alt rs62516141(G;G)
Reference rs62516141(A;A)
Significance Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103237466T>C
CLNSRC
CLNACC RCV000088771.3, RCV000169306.1,