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rs62509017

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 Carrier of a phenylketonuria mutation
Make rs62509017(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102894846
GenePAH
is asnp
is mentioned by
dbSNPrs62509017
ebirs62509017
HLIrs62509017
Exacrs62509017
Varsomers62509017
Maprs62509017
PheGenIrs62509017
hapmaprs62509017
1000 genomesrs62509017
hgdprs62509017
ensemblrs62509017
gopubmedrs62509017
geneviewrs62509017
scholarrs62509017
googlers62509017
pharmgkbrs62509017
gwascentralrs62509017
openSNPrs62509017
23andMers62509017
23andMe allrs62509017
SNP Nexus

SNPshotrs62509017
SNPdbers62509017
MSV3drs62509017
GWAS Ctlgrs62509017
Max Magnitude3
ClinVar
Risk rs62509017(C;C)
Alt rs62509017(C;C)
Reference rs62509017(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103288624T>G
CLNSRC
CLNACC RCV000088881.1,