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rs63102461

From SNPedia

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


Make rs63102461(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102866595
GenePAH
is asnp
is mentioned by
dbSNPrs63102461
ebirs63102461
HLIrs63102461
Exacrs63102461
Varsomers63102461
Maprs63102461
PheGenIrs63102461
hapmaprs63102461
1000 genomesrs63102461
hgdprs63102461
ensemblrs63102461
gopubmedrs63102461
geneviewrs63102461
scholarrs63102461
googlers63102461
pharmgkbrs63102461
gwascentralrs63102461
openSNPrs63102461
23andMers63102461
23andMe allrs63102461
SNP Nexus

SNPshotrs63102461
SNPdbers63102461
MSV3drs63102461
GWAS Ctlgrs63102461
Max Magnitude3
ClinVar
Risk rs63102461(A;A)
Alt rs63102461(A;A)
Reference rs63102461(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103260373C>T
CLNSRC
CLNACC RCV000088955.1,