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rs62507286

From SNPedia

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


Make rs62507286(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852843
GenePAH
is asnp
is mentioned by
dbSNPrs62507286
ebirs62507286
HLIrs62507286
Exacrs62507286
Varsomers62507286
Maprs62507286
PheGenIrs62507286
hapmaprs62507286
1000 genomesrs62507286
hgdprs62507286
ensemblrs62507286
gopubmedrs62507286
geneviewrs62507286
scholarrs62507286
googlers62507286
pharmgkbrs62507286
gwascentralrs62507286
openSNPrs62507286
23andMers62507286
23andMe allrs62507286
SNP Nexus

SNPshotrs62507286
SNPdbers62507286
MSV3drs62507286
GWAS Ctlgrs62507286
Max Magnitude3
ClinVar
Risk rs62507286(;)
Alt rs62507286(;)
Reference rs62507286(ACATG;ACATG)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246621_103246625delCATGT
CLNSRC
CLNACC RCV000089107.1,