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rs62507282

From SNPedia

Orientationminus
Geno Mag Summary
(C;G) 3 Carrier of a phenylketonuria mutation
(G;G) 0 common in clinvar
Make rs62507282(A;A)
Make rs62507282(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102844377
GenePAH
is asnp
is mentioned by
dbSNPrs62507282
ebirs62507282
HLIrs62507282
Exacrs62507282
Varsomers62507282
Maprs62507282
PheGenIrs62507282
hapmaprs62507282
1000 genomesrs62507282
hgdprs62507282
ensemblrs62507282
gopubmedrs62507282
geneviewrs62507282
scholarrs62507282
googlers62507282
pharmgkbrs62507282
gwascentralrs62507282
openSNPrs62507282
23andMers62507282
23andMe allrs62507282
SNP Nexus

SNPshotrs62507282
SNPdbers62507282
MSV3drs62507282
GWAS Ctlgrs62507282
Max Magnitude3
ClinVar
Risk rs62507282(A,C;A,C)
Alt rs62507282(A,C;A,C)
Reference rs62507282(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103238155C>G; NC_000012.11:g.103238155C>T
CLNSRC
CLNACC RCV000088705.1, RCV000088704.1,