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rs62508649

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs62508649(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102840396
GenePAH
is asnp
is mentioned by
dbSNPrs62508649
ebirs62508649
HLIrs62508649
Exacrs62508649
Varsomers62508649
Maprs62508649
PheGenIrs62508649
hapmaprs62508649
1000 genomesrs62508649
hgdprs62508649
ensemblrs62508649
gopubmedrs62508649
geneviewrs62508649
scholarrs62508649
googlers62508649
pharmgkbrs62508649
gwascentralrs62508649
openSNPrs62508649
23andMers62508649
23andMe allrs62508649
SNP Nexus

SNPshotrs62508649
SNPdbers62508649
MSV3drs62508649
GWAS Ctlgrs62508649
Max Magnitude3
ClinVar
Risk rs62508649(G;G)
Alt rs62508649(G;G)
Reference rs62508649(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103234174T>C
CLNSRC
CLNACC RCV000088828.1,