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rs62507269

From SNPedia

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


Make rs62507269(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852951
GenePAH
is asnp
is mentioned by
dbSNPrs62507269
ebirs62507269
HLIrs62507269
Exacrs62507269
Varsomers62507269
Maprs62507269
PheGenIrs62507269
hapmaprs62507269
1000 genomesrs62507269
hgdprs62507269
ensemblrs62507269
gopubmedrs62507269
geneviewrs62507269
scholarrs62507269
googlers62507269
pharmgkbrs62507269
gwascentralrs62507269
openSNPrs62507269
23andMers62507269
23andMe allrs62507269
SNP Nexus

SNPshotrs62507269
SNPdbers62507269
MSV3drs62507269
GWAS Ctlgrs62507269
Max Magnitude3
ClinVar
Risk rs62507269(A;A)
Alt rs62507269(A;A)
Reference rs62507269(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246729C>T
CLNSRC
CLNACC RCV000089044.1,