Have questions? Visit https://www.reddit.com/r/SNPedia

rs63083560

From SNPedia

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


Make rs63083560(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855229
GenePAH
is asnp
is mentioned by
dbSNPrs63083560
ebirs63083560
HLIrs63083560
Exacrs63083560
Varsomers63083560
Maprs63083560
PheGenIrs63083560
hapmaprs63083560
1000 genomesrs63083560
hgdprs63083560
ensemblrs63083560
gopubmedrs63083560
geneviewrs63083560
scholarrs63083560
googlers63083560
pharmgkbrs63083560
gwascentralrs63083560
openSNPrs63083560
23andMers63083560
23andMe allrs63083560
SNP Nexus

SNPshotrs63083560
SNPdbers63083560
MSV3drs63083560
GWAS Ctlgrs63083560
Max Magnitude3
ClinVar
Risk rs63083560(A;A)
Alt rs63083560(A;A)
Reference rs63083560(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103249007C>T
CLNSRC
CLNACC RCV000089009.1,