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

rs62507264

From SNPedia

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


Make rs62507264(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102846956
GenePAH
is asnp
is mentioned by
dbSNPrs62507264
ebirs62507264
HLIrs62507264
Exacrs62507264
Varsomers62507264
Maprs62507264
PheGenIrs62507264
hapmaprs62507264
1000 genomesrs62507264
hgdprs62507264
ensemblrs62507264
gopubmedrs62507264
geneviewrs62507264
scholarrs62507264
googlers62507264
pharmgkbrs62507264
gwascentralrs62507264
openSNPrs62507264
23andMers62507264
23andMe allrs62507264
SNP Nexus

SNPshotrs62507264
SNPdbers62507264
MSV3drs62507264
GWAS Ctlgrs62507264
Max Magnitude3
ClinVar
Risk rs62507264(C,G;C,G)
Alt rs62507264(C,G;C,G)
Reference rs62507264(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103240734A>C
CLNSRC
CLNACC RCV000089155.1,