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

rs869312997

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312997(C;C)
Make rs869312997(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843673
GenePAH
is asnp
is mentioned by
dbSNPrs869312997
ebirs869312997
HLIrs869312997
Exacrs869312997
Varsomers869312997
Maprs869312997
PheGenIrs869312997
hapmaprs869312997
1000 genomesrs869312997
hgdprs869312997
ensemblrs869312997
gopubmedrs869312997
geneviewrs869312997
scholarrs869312997
googlers869312997
pharmgkbrs869312997
gwascentralrs869312997
openSNPrs869312997
23andMers869312997
23andMe allrs869312997
SNP Nexus

SNPshotrs869312997
SNPdbers869312997
MSV3drs869312997
GWAS Ctlgrs869312997
Max Magnitude0
ClinVar
Risk rs869312997(C;C)
Alt rs869312997(C;C)
Reference rs869312997(G;G)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103237451C>G
CLNSRC
CLNACC RCV000210788.1,