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rs199475629

From SNPedia

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


Make rs199475629(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843681
GenePAH
is asnp
is mentioned by
dbSNPrs199475629
ebirs199475629
HLIrs199475629
Exacrs199475629
Varsomers199475629
Maprs199475629
PheGenIrs199475629
hapmaprs199475629
1000 genomesrs199475629
hgdprs199475629
ensemblrs199475629
gopubmedrs199475629
geneviewrs199475629
scholarrs199475629
googlers199475629
pharmgkbrs199475629
gwascentralrs199475629
openSNPrs199475629
23andMers199475629
23andMe allrs199475629
SNP Nexus

SNPshotrs199475629
SNPdbers199475629
MSV3drs199475629
GWAS Ctlgrs199475629
Max Magnitude3
ClinVar
Risk rs199475629(;)
Alt rs199475629(;)
Reference rs199475629(TG;TG)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237459_103237460delCA
CLNSRC
CLNACC RCV000088776.1,