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

rs62507332

From SNPedia

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


Make rs62507332(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102894856
GenePAH
is asnp
is mentioned by
dbSNPrs62507332
ebirs62507332
HLIrs62507332
Exacrs62507332
Varsomers62507332
Maprs62507332
PheGenIrs62507332
hapmaprs62507332
1000 genomesrs62507332
hgdprs62507332
ensemblrs62507332
gopubmedrs62507332
geneviewrs62507332
scholarrs62507332
googlers62507332
pharmgkbrs62507332
gwascentralrs62507332
openSNPrs62507332
23andMers62507332
23andMe allrs62507332
SNP Nexus

SNPshotrs62507332
SNPdbers62507332
MSV3drs62507332
GWAS Ctlgrs62507332
Max Magnitude3
ClinVar
Risk rs62507332(C,G;C,G)
Alt rs62507332(C,G;C,G)
Reference rs62507332(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103288634A>C
CLNSRC
CLNACC RCV000088879.1,