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rs62507260

From SNPedia

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


Make rs62507260(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855279
GenePAH
is asnp
is mentioned by
dbSNPrs62507260
ebirs62507260
HLIrs62507260
Exacrs62507260
Varsomers62507260
Maprs62507260
PheGenIrs62507260
hapmaprs62507260
1000 genomesrs62507260
hgdprs62507260
ensemblrs62507260
gopubmedrs62507260
geneviewrs62507260
scholarrs62507260
googlers62507260
pharmgkbrs62507260
gwascentralrs62507260
openSNPrs62507260
23andMers62507260
23andMe allrs62507260
SNP Nexus

SNPshotrs62507260
SNPdbers62507260
MSV3drs62507260
GWAS Ctlgrs62507260
Max Magnitude3
ClinVar
Risk rs62507260(;)
Alt rs62507260(;)
Reference rs62507260(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103249057delC
CLNSRC
CLNACC RCV000088988.1,