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rs62517183

From SNPedia

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


Make rs62517183(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844353
GenePAH
is asnp
is mentioned by
dbSNPrs62517183
ebirs62517183
HLIrs62517183
Exacrs62517183
Varsomers62517183
Maprs62517183
PheGenIrs62517183
hapmaprs62517183
1000 genomesrs62517183
hgdprs62517183
ensemblrs62517183
gopubmedrs62517183
geneviewrs62517183
scholarrs62517183
googlers62517183
pharmgkbrs62517183
gwascentralrs62517183
openSNPrs62517183
23andMers62517183
23andMe allrs62517183
SNP Nexus

SNPshotrs62517183
SNPdbers62517183
MSV3drs62517183
GWAS Ctlgrs62517183
Max Magnitude3
ClinVar
Risk rs62517183(A;A)
Alt rs62517183(A;A)
Reference rs62517183(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238131A>T
CLNSRC
CLNACC RCV000088725.1,