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rs199475656

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 3 Carrier of a phenylketonuria mutation
Make rs199475656(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855138
GenePAH
is asnp
is mentioned by
dbSNPrs199475656
ebirs199475656
HLIrs199475656
Exacrs199475656
Varsomers199475656
Maprs199475656
PheGenIrs199475656
hapmaprs199475656
1000 genomesrs199475656
hgdprs199475656
ensemblrs199475656
gopubmedrs199475656
geneviewrs199475656
scholarrs199475656
googlers199475656
pharmgkbrs199475656
gwascentralrs199475656
openSNPrs199475656
23andMers199475656
23andMe allrs199475656
SNP Nexus

SNPshotrs199475656
SNPdbers199475656
MSV3drs199475656
GWAS Ctlgrs199475656
Max Magnitude3
ClinVar
Risk rs199475656(C;C)
Alt rs199475656(C;C)
Reference rs199475656(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103248916T>G
CLNSRC
CLNACC RCV000089042.1,