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rs62508650

From SNPedia

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


Make rs62508650(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102840394
GenePAH
is asnp
is mentioned by
dbSNPrs62508650
ebirs62508650
HLIrs62508650
Exacrs62508650
Varsomers62508650
Maprs62508650
PheGenIrs62508650
hapmaprs62508650
1000 genomesrs62508650
hgdprs62508650
ensemblrs62508650
gopubmedrs62508650
geneviewrs62508650
scholarrs62508650
googlers62508650
pharmgkbrs62508650
gwascentralrs62508650
openSNPrs62508650
23andMers62508650
23andMe allrs62508650
SNP Nexus

SNPshotrs62508650
SNPdbers62508650
MSV3drs62508650
GWAS Ctlgrs62508650
Max Magnitude3
ClinVar
Risk rs62508650(A;A)
Alt rs62508650(A;A)
Reference rs62508650(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103234172A>T
CLNSRC
CLNACC RCV000088829.1,