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rs138809906

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs138809906(A;T)
Make rs138809906(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855321
GenePAH
is asnp
is mentioned by
dbSNPrs138809906
ebirs138809906
HLIrs138809906
Exacrs138809906
Varsomers138809906
Maprs138809906
PheGenIrs138809906
hapmaprs138809906
1000 genomesrs138809906
hgdprs138809906
ensemblrs138809906
gopubmedrs138809906
geneviewrs138809906
scholarrs138809906
googlers138809906
pharmgkbrs138809906
gwascentralrs138809906
openSNPrs138809906
23andMers138809906
23andMe allrs138809906
SNP Nexus

SNPshotrs138809906
SNPdbers138809906
MSV3drs138809906
GWAS Ctlgrs138809906
Max Magnitude3
ClinVar
Risk rs138809906(G,T;G,T)
Alt rs138809906(G,T;G,T)
Reference rs138809906(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.103249099A>G
CLNSRC
CLNACC RCV000088969.1,