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rs62508573

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Carrier of a phenylketonuria mutation
Make rs62508573(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844426
GenePAH
is asnp
is mentioned by
dbSNPrs62508573
ebirs62508573
HLIrs62508573
Exacrs62508573
Varsomers62508573
Maprs62508573
PheGenIrs62508573
hapmaprs62508573
1000 genomesrs62508573
hgdprs62508573
ensemblrs62508573
gopubmedrs62508573
geneviewrs62508573
scholarrs62508573
googlers62508573
pharmgkbrs62508573
gwascentralrs62508573
openSNPrs62508573
23andMers62508573
23andMe allrs62508573
SNP Nexus

SNPshotrs62508573
SNPdbers62508573
MSV3drs62508573
GWAS Ctlgrs62508573
Max Magnitude3
ClinVar
Risk rs62508573(G;G)
Alt rs62508573(G;G)
Reference rs62508573(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238204G>C
CLNSRC
CLNACC RCV000089187.1,