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rs199475687

From SNPedia

Orientationminus
Geno Mag Summary
(-;CTT) 3 Carrier of a phenylketonuria mutation
(TCT;TCT) 0 common in clinvar
Make rs199475687(-;-)
Make rs199475687(CTT;CTT)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102894879
GenePAH
is asnp
is mentioned by
dbSNPrs199475687
ebirs199475687
HLIrs199475687
Exacrs199475687
Varsomers199475687
Maprs199475687
PheGenIrs199475687
hapmaprs199475687
1000 genomesrs199475687
hgdprs199475687
ensemblrs199475687
gopubmedrs199475687
geneviewrs199475687
scholarrs199475687
googlers199475687
pharmgkbrs199475687
gwascentralrs199475687
openSNPrs199475687
23andMers199475687
23andMe allrs199475687
SNP Nexus

SNPshotrs199475687
SNPdbers199475687
MSV3drs199475687
GWAS Ctlgrs199475687
Max Magnitude3
ClinVar
Risk rs199475687(;)
Alt rs199475687(;)
Reference rs199475687(TCT;TCT)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103288655_103288657delAGA
CLNSRC
CLNACC RCV000088875.2,