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rs199475681

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199475681(G;T)
Make rs199475681(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102877535
GenePAH
is asnp
is mentioned by
dbSNPrs199475681
ebirs199475681
HLIrs199475681
Exacrs199475681
Varsomers199475681
Maprs199475681
PheGenIrs199475681
hapmaprs199475681
1000 genomesrs199475681
hgdprs199475681
ensemblrs199475681
gopubmedrs199475681
geneviewrs199475681
scholarrs199475681
googlers199475681
pharmgkbrs199475681
gwascentralrs199475681
openSNPrs199475681
23andMers199475681
23andMe allrs199475681
SNP Nexus

SNPshotrs199475681
SNPdbers199475681
MSV3drs199475681
GWAS Ctlgrs199475681
Max Magnitude0
ClinVar
Risk rs199475681(T;T)
Alt rs199475681(T;T)
Reference rs199475681(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103271313C>A
CLNSRC
CLNACC RCV000088905.2,