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rs199475586

From SNPedia

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


Make rs199475586(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102877544
GenePAH
is asnp
is mentioned by
dbSNPrs199475586
ebirs199475586
HLIrs199475586
Exacrs199475586
Varsomers199475586
Maprs199475586
PheGenIrs199475586
hapmaprs199475586
1000 genomesrs199475586
hgdprs199475586
ensemblrs199475586
gopubmedrs199475586
geneviewrs199475586
scholarrs199475586
googlers199475586
pharmgkbrs199475586
gwascentralrs199475586
openSNPrs199475586
23andMers199475586
23andMe allrs199475586
SNP Nexus

SNPshotrs199475586
SNPdbers199475586
MSV3drs199475586
GWAS Ctlgrs199475586
Max Magnitude3
ClinVar
Risk rs199475586(A;A)
Alt rs199475586(A;A)
Reference rs199475586(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103271322C>T
CLNSRC
CLNACC RCV000088903.1,