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rs62642921

From SNPedia

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


Make rs62642921(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843718
GenePAH
is asnp
is mentioned by
dbSNPrs62642921
ebirs62642921
HLIrs62642921
Exacrs62642921
Varsomers62642921
Maprs62642921
PheGenIrs62642921
hapmaprs62642921
1000 genomesrs62642921
hgdprs62642921
ensemblrs62642921
gopubmedrs62642921
geneviewrs62642921
scholarrs62642921
googlers62642921
pharmgkbrs62642921
gwascentralrs62642921
openSNPrs62642921
23andMers62642921
23andMe allrs62642921
SNP Nexus

SNPshotrs62642921
SNPdbers62642921
MSV3drs62642921
GWAS Ctlgrs62642921
Max Magnitude3
ClinVar
Risk rs62642921(;)
Alt rs62642921(;)
Reference rs62642921(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237496delT
CLNSRC
CLNACC RCV000088765.1,