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rs62508586

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs62508586(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102877458
GenePAH
is asnp
is mentioned by
dbSNPrs62508586
ebirs62508586
HLIrs62508586
Exacrs62508586
Varsomers62508586
Maprs62508586
PheGenIrs62508586
hapmaprs62508586
1000 genomesrs62508586
hgdprs62508586
ensemblrs62508586
gopubmedrs62508586
geneviewrs62508586
scholarrs62508586
googlers62508586
pharmgkbrs62508586
gwascentralrs62508586
openSNPrs62508586
23andMers62508586
23andMe allrs62508586
SNP Nexus

SNPshotrs62508586
SNPdbers62508586
MSV3drs62508586
GWAS Ctlgrs62508586
Max Magnitude3
ClinVar
Risk rs62508586(G;G)
Alt rs62508586(G;G)
Reference rs62508586(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103271236T>C
CLNSRC
CLNACC RCV000088922.1,