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

rs281865429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;C) 3 Carrier of a phenylketonuria mutation
(C;C) 0 common in clinvar


Make rs281865429(-;-)
ReferenceGRCh38 38.1/142
Chromosome12
Position102852820
GenePAH
is asnp
is mentioned by
dbSNPrs281865429
ebirs281865429
HLIrs281865429
Exacrs281865429
Varsomers281865429
Maprs281865429
PheGenIrs281865429
hapmaprs281865429
1000 genomesrs281865429
hgdprs281865429
ensemblrs281865429
gopubmedrs281865429
geneviewrs281865429
scholarrs281865429
googlers281865429
pharmgkbrs281865429
gwascentralrs281865429
openSNPrs281865429
23andMers281865429
23andMe allrs281865429
SNP Nexus

SNPshotrs281865429
SNPdbers281865429
MSV3drs281865429
GWAS Ctlgrs281865429
Max Magnitude3
ClinVar
Risk rs281865429(;)
Alt rs281865429(;)
Reference rs281865429(C;C)
Significance Probable-Pathogenic
Disease Phenylketonuria
Variation info
Gene PAH
CLNDBN Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103246598delG
CLNSRC ClinVar
CLNACC RCV000106369.1,