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rs199475679

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199475679(A;A)
Make rs199475679(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102866599
GenePAH
is asnp
is mentioned by
dbSNPrs199475679
ebirs199475679
HLIrs199475679
Exacrs199475679
Varsomers199475679
Maprs199475679
PheGenIrs199475679
hapmaprs199475679
1000 genomesrs199475679
hgdprs199475679
ensemblrs199475679
gopubmedrs199475679
geneviewrs199475679
scholarrs199475679
googlers199475679
pharmgkbrs199475679
gwascentralrs199475679
openSNPrs199475679
23andMers199475679
23andMe allrs199475679
SNP Nexus

SNPshotrs199475679
SNPdbers199475679
MSV3drs199475679
GWAS Ctlgrs199475679
Max Magnitude0
ClinVar
Risk rs199475679(A;A)
Alt rs199475679(A;A)
Reference rs199475679(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103260377C>T
CLNSRC
CLNACC RCV000088954.2,