Have questions? Visit https://www.reddit.com/r/SNPedia

rs62516151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62516151(A;A)
Make rs62516151(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position102894826
GenePAH
is asnp
is mentioned by
dbSNPrs62516151
ebirs62516151
HLIrs62516151
Exacrs62516151
Varsomers62516151
Maprs62516151
PheGenIrs62516151
hapmaprs62516151
1000 genomesrs62516151
hgdprs62516151
ensemblrs62516151
gopubmedrs62516151
geneviewrs62516151
scholarrs62516151
googlers62516151
pharmgkbrs62516151
gwascentralrs62516151
openSNPrs62516151
23andMers62516151
23andMe allrs62516151
SNP Nexus

SNPshotrs62516151
SNPdbers62516151
MSV3drs62516151
GWAS Ctlgrs62516151
Max Magnitude0
OMIM612349
Desc
Variant0057
Relatedalso
ClinVar
Risk rs62516151(A;A)
Alt rs62516151(A;A)
Reference rs62516151(C;C)
Significance Pathogenic
Disease Hyperphenylalaninemia not provided
Variation info
Gene PAH
CLNDBN Hyperphenylalaninemia, non-pku not provided
Reversed 1
HGVS NC_000012.11:g.103288604G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000613.3, RCV000088884.2,