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rs62509019

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 3 Carrier of a phenylketonuria mutation
Make rs62509019(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102851758
GenePAH
is asnp
is mentioned by
dbSNPrs62509019
ebirs62509019
HLIrs62509019
Exacrs62509019
Varsomers62509019
Maprs62509019
PheGenIrs62509019
hapmaprs62509019
1000 genomesrs62509019
hgdprs62509019
ensemblrs62509019
gopubmedrs62509019
geneviewrs62509019
scholarrs62509019
googlers62509019
pharmgkbrs62509019
gwascentralrs62509019
openSNPrs62509019
23andMers62509019
23andMe allrs62509019
SNP Nexus

SNPshotrs62509019
SNPdbers62509019
MSV3drs62509019
GWAS Ctlgrs62509019
Max Magnitude3
ClinVar
Risk rs62509019(T;T)
Alt rs62509019(T;T)
Reference rs62509019(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103245536T>A
CLNSRC
CLNACC RCV000089134.1,