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rs62508620

From SNPedia

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


Make rs62508620(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102843746
GenePAH
is asnp
is mentioned by
dbSNPrs62508620
ebirs62508620
HLIrs62508620
Exacrs62508620
Varsomers62508620
Maprs62508620
PheGenIrs62508620
hapmaprs62508620
1000 genomesrs62508620
hgdprs62508620
ensemblrs62508620
gopubmedrs62508620
geneviewrs62508620
scholarrs62508620
googlers62508620
pharmgkbrs62508620
gwascentralrs62508620
openSNPrs62508620
23andMers62508620
23andMe allrs62508620
SNP Nexus

SNPshotrs62508620
SNPdbers62508620
MSV3drs62508620
GWAS Ctlgrs62508620
Max Magnitude3
ClinVar
Risk rs62508620(;)
Alt rs62508620(;)
Reference rs62508620(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103237524delG
CLNSRC
CLNACC RCV000088757.1,