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rs62642932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 6 Phenyketonuria
(A;G) 3 Carrier of a phenylketonuria mutation
(G;G) 0 common/normal
ReferenceGRCh38 38.1/142
Chromosome12
Position102852882
GenePAH
is asnp
is mentioned by
dbSNPrs62642932
ebirs62642932
HLIrs62642932
Exacrs62642932
Varsomers62642932
Maprs62642932
PheGenIrs62642932
hapmaprs62642932
1000 genomesrs62642932
hgdprs62642932
ensemblrs62642932
gopubmedrs62642932
geneviewrs62642932
scholarrs62642932
googlers62642932
pharmgkbrs62642932
gwascentralrs62642932
openSNPrs62642932
23andMers62642932
23andMe allrs62642932
SNP Nexus

SNPshotrs62642932
SNPdbers62642932
MSV3drs62642932
GWAS Ctlgrs62642932
Max Magnitude6


ClinVar
Risk rs62642932(A;A)
Alt rs62642932(A;A)
Reference rs62642932(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246660C>T
CLNSRC ClinVar DeBelle Laboratory for Biochemical Genetics
CLNACC RCV000089088.1,