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rs62506949

From SNPedia

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


Make rs62506949(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843679
GenePAH
is asnp
is mentioned by
dbSNPrs62506949
ebirs62506949
HLIrs62506949
Exacrs62506949
Varsomers62506949
Maprs62506949
PheGenIrs62506949
hapmaprs62506949
1000 genomesrs62506949
hgdprs62506949
ensemblrs62506949
gopubmedrs62506949
geneviewrs62506949
scholarrs62506949
googlers62506949
pharmgkbrs62506949
gwascentralrs62506949
openSNPrs62506949
23andMers62506949
23andMe allrs62506949
SNP Nexus

SNPshotrs62506949
SNPdbers62506949
MSV3drs62506949
GWAS Ctlgrs62506949
Max Magnitude3
ClinVar
Risk rs62506949(;)
Alt rs62506949(;)
Reference rs62506949(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237457delG
CLNSRC
CLNACC RCV000088777.1,