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rs74503222

From SNPedia

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


Make rs74503222(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102852912
GenePAH
is asnp
is mentioned by
dbSNPrs74503222
ebirs74503222
HLIrs74503222
Exacrs74503222
Varsomers74503222
Maprs74503222
PheGenIrs74503222
hapmaprs74503222
1000 genomesrs74503222
hgdprs74503222
ensemblrs74503222
gopubmedrs74503222
geneviewrs74503222
scholarrs74503222
googlers74503222
pharmgkbrs74503222
gwascentralrs74503222
openSNPrs74503222
23andMers74503222
23andMe allrs74503222
SNP Nexus

SNPshotrs74503222
SNPdbers74503222
MSV3drs74503222
GWAS Ctlgrs74503222
Max Magnitude3
ClinVar
Risk rs74503222(A;A)
Alt rs74503222(A;A)
Reference rs74503222(G;G)
Significance Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 0
HGVS NC_000012.11:g.103246690G>A
CLNSRC HGMD
CLNACC RCV000089076.2, RCV000153634.3,