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rs62507267

From SNPedia

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


Make rs62507267(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102851702
GenePAH
is asnp
is mentioned by
dbSNPrs62507267
ebirs62507267
HLIrs62507267
Exacrs62507267
Varsomers62507267
Maprs62507267
PheGenIrs62507267
hapmaprs62507267
1000 genomesrs62507267
hgdprs62507267
ensemblrs62507267
gopubmedrs62507267
geneviewrs62507267
scholarrs62507267
googlers62507267
pharmgkbrs62507267
gwascentralrs62507267
openSNPrs62507267
23andMers62507267
23andMe allrs62507267
SNP Nexus

SNPshotrs62507267
SNPdbers62507267
MSV3drs62507267
GWAS Ctlgrs62507267
Max Magnitude3
ClinVar
Risk rs62507267(;)
Alt rs62507267(;)
Reference rs62507267(TTT;TTT)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103245480_103245482delAAA
CLNSRC
CLNACC RCV000089147.1,