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rs62507350

From SNPedia

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


Make rs62507350(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844345
GenePAH
is asnp
is mentioned by
dbSNPrs62507350
ebirs62507350
HLIrs62507350
Exacrs62507350
Varsomers62507350
Maprs62507350
PheGenIrs62507350
hapmaprs62507350
1000 genomesrs62507350
hgdprs62507350
ensemblrs62507350
gopubmedrs62507350
geneviewrs62507350
scholarrs62507350
googlers62507350
pharmgkbrs62507350
gwascentralrs62507350
openSNPrs62507350
23andMers62507350
23andMe allrs62507350
SNP Nexus

SNPshotrs62507350
SNPdbers62507350
MSV3drs62507350
GWAS Ctlgrs62507350
Max Magnitude3
ClinVar
Risk rs62507350(;)
Alt rs62507350(;)
Reference rs62507350(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238123delA
CLNSRC
CLNACC RCV000088730.1,