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

rs62507283

From SNPedia

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


Make rs62507283(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852941
GenePAH
is asnp
is mentioned by
dbSNPrs62507283
ebirs62507283
HLIrs62507283
Exacrs62507283
Varsomers62507283
Maprs62507283
PheGenIrs62507283
hapmaprs62507283
1000 genomesrs62507283
hgdprs62507283
ensemblrs62507283
gopubmedrs62507283
geneviewrs62507283
scholarrs62507283
googlers62507283
pharmgkbrs62507283
gwascentralrs62507283
openSNPrs62507283
23andMers62507283
23andMe allrs62507283
SNP Nexus

SNPshotrs62507283
SNPdbers62507283
MSV3drs62507283
GWAS Ctlgrs62507283
Max Magnitude3
ClinVar
Risk rs62507283(A,C,T;A,C,T)
Alt rs62507283(A,C,T;A,C,T)
Reference rs62507283(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246719C>A; NC_000012.11:g.103246719C>G; NC_000012.11:g.103246719C>T
CLNSRC HGMD
CLNACC RCV000089051.4, RCV000089050.1, RCV000089049.1,