Have questions? Visit https://www.reddit.com/r/SNPedia

rs62508587

From SNPedia

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


Make rs62508587(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102855261
GenePAH
is asnp
is mentioned by
dbSNPrs62508587
ebirs62508587
HLIrs62508587
Exacrs62508587
Varsomers62508587
Maprs62508587
PheGenIrs62508587
hapmaprs62508587
1000 genomesrs62508587
hgdprs62508587
ensemblrs62508587
gopubmedrs62508587
geneviewrs62508587
scholarrs62508587
googlers62508587
pharmgkbrs62508587
gwascentralrs62508587
openSNPrs62508587
23andMers62508587
23andMe allrs62508587
SNP Nexus

SNPshotrs62508587
SNPdbers62508587
MSV3drs62508587
GWAS Ctlgrs62508587
Max Magnitude3
ClinVar
Risk rs62508587(;)
Alt rs62508587(;)
Reference rs62508587(CT;CT)
Significance Probable-Pathogenic
Disease not provided Phenylketonuria
Variation info
Gene PAH
CLNDBN not provided Phenylketonuria
Reversed 1
HGVS NC_000012.11:g.103249039_103249040delAG
CLNSRC
CLNACC RCV000088990.1, RCV000169180.1,