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rs62517168

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs62517168(A;T)
Make rs62517168(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102851752
GenePAH
is asnp
is mentioned by
dbSNPrs62517168
ebirs62517168
HLIrs62517168
Exacrs62517168
Varsomers62517168
Maprs62517168
PheGenIrs62517168
hapmaprs62517168
1000 genomesrs62517168
hgdprs62517168
ensemblrs62517168
gopubmedrs62517168
geneviewrs62517168
scholarrs62517168
googlers62517168
pharmgkbrs62517168
gwascentralrs62517168
openSNPrs62517168
23andMers62517168
23andMe allrs62517168
SNP Nexus

SNPshotrs62517168
SNPdbers62517168
MSV3drs62517168
GWAS Ctlgrs62517168
Max Magnitude0
ClinVar
Risk rs62517168(T;T)
Alt rs62517168(T;T)
Reference rs62517168(A;A)
Significance Probable-Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103245530T>A
CLNSRC
CLNACC RCV000089137.1, RCV000169005.1,