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rs762462102

From SNPedia

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Geno Mag Summary
(-;AGA) 3 Carrier of a phenylketonuria mutation
Make rs762462102(-;-)
Make rs762462102(AGA;AGA)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102912841
GenePAH
is asnp
is mentioned by
dbSNPrs762462102
ebirs762462102
HLIrs762462102
Exacrs762462102
Varsomers762462102
Maprs762462102
PheGenIrs762462102
hapmaprs762462102
1000 genomesrs762462102
hgdprs762462102
ensemblrs762462102
gopubmedrs762462102
geneviewrs762462102
scholarrs762462102
googlers762462102
pharmgkbrs762462102
gwascentralrs762462102
openSNPrs762462102
23andMers762462102
23andMe allrs762462102
SNP Nexus

SNPshotrs762462102
SNPdbers762462102
MSV3drs762462102
GWAS Ctlgrs762462102
Max Magnitude3
ClinVar
Risk rs762462102(;)
Alt rs762462102(;)
Reference rs762462102(AGA;AGA)
Significance Other
Disease Phenylketonuria not provided
Variation info
Gene PAH
CLNDBN Phenylketonuria not provided
Reversed 0
HGVS NC_000012.11:g.103306619_103306621delAGA
CLNSRC
CLNACC RCV000169302.2, RCV000186077.1,