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rs62508684

From SNPedia

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


Make rs62508684(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843780
GenePAH
is asnp
is mentioned by
dbSNPrs62508684
ebirs62508684
HLIrs62508684
Exacrs62508684
Varsomers62508684
Maprs62508684
PheGenIrs62508684
hapmaprs62508684
1000 genomesrs62508684
hgdprs62508684
ensemblrs62508684
gopubmedrs62508684
geneviewrs62508684
scholarrs62508684
googlers62508684
pharmgkbrs62508684
gwascentralrs62508684
openSNPrs62508684
23andMers62508684
23andMe allrs62508684
SNP Nexus

SNPshotrs62508684
SNPdbers62508684
MSV3drs62508684
GWAS Ctlgrs62508684
Max Magnitude3
ClinVar
Risk rs62508684(A;A)
Alt rs62508684(A;A)
Reference rs62508684(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237558C>T
CLNSRC
CLNACC RCV000088740.1,