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rs62514911

From SNPedia

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


Make rs62514911(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102866595
GenePAH
is asnp
is mentioned by
dbSNPrs62514911
ebirs62514911
HLIrs62514911
Exacrs62514911
Varsomers62514911
Maprs62514911
PheGenIrs62514911
hapmaprs62514911
1000 genomesrs62514911
hgdprs62514911
ensemblrs62514911
gopubmedrs62514911
geneviewrs62514911
scholarrs62514911
googlers62514911
pharmgkbrs62514911
gwascentralrs62514911
openSNPrs62514911
23andMers62514911
23andMe allrs62514911
SNP Nexus

SNPshotrs62514911
SNPdbers62514911
MSV3drs62514911
GWAS Ctlgrs62514911
Max Magnitude3
ClinVar
Risk rs62514911(;)
Alt rs62514911(;)
Reference rs62514911(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103260373delC
CLNSRC
CLNACC RCV000088956.1,