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rs62507274

From SNPedia

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


Make rs62507274(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844437
GenePAH
is asnp
is mentioned by
dbSNPrs62507274
ebirs62507274
HLIrs62507274
Exacrs62507274
Varsomers62507274
Maprs62507274
PheGenIrs62507274
hapmaprs62507274
1000 genomesrs62507274
hgdprs62507274
ensemblrs62507274
gopubmedrs62507274
geneviewrs62507274
scholarrs62507274
googlers62507274
pharmgkbrs62507274
gwascentralrs62507274
openSNPrs62507274
23andMers62507274
23andMe allrs62507274
SNP Nexus

SNPshotrs62507274
SNPdbers62507274
MSV3drs62507274
GWAS Ctlgrs62507274
Max Magnitude3
ClinVar
Risk rs62507274(G;G)
Alt rs62507274(G;G)
Reference rs62507274(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238215A>C
CLNSRC
CLNACC RCV000089186.1,