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rs62516099

From SNPedia

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


Make rs62516099(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843727
GenePAH
is asnp
is mentioned by
dbSNPrs62516099
ebirs62516099
HLIrs62516099
Exacrs62516099
Varsomers62516099
Maprs62516099
PheGenIrs62516099
hapmaprs62516099
1000 genomesrs62516099
hgdprs62516099
ensemblrs62516099
gopubmedrs62516099
geneviewrs62516099
scholarrs62516099
googlers62516099
pharmgkbrs62516099
gwascentralrs62516099
openSNPrs62516099
23andMers62516099
23andMe allrs62516099
SNP Nexus

SNPshotrs62516099
SNPdbers62516099
MSV3drs62516099
GWAS Ctlgrs62516099
Max Magnitude3
ClinVar
Risk rs62516099(;)
Alt rs62516099(;)
Reference rs62516099(GC;GC)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237505_103237506delGC
CLNSRC
CLNACC RCV000088763.1,