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

rs62507324

From SNPedia

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


Make rs62507324(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852812
GenePAH
is asnp
is mentioned by
dbSNPrs62507324
ebirs62507324
HLIrs62507324
Exacrs62507324
Varsomers62507324
Maprs62507324
PheGenIrs62507324
hapmaprs62507324
1000 genomesrs62507324
hgdprs62507324
ensemblrs62507324
gopubmedrs62507324
geneviewrs62507324
scholarrs62507324
googlers62507324
pharmgkbrs62507324
gwascentralrs62507324
openSNPrs62507324
23andMers62507324
23andMe allrs62507324
SNP Nexus

SNPshotrs62507324
SNPdbers62507324
MSV3drs62507324
GWAS Ctlgrs62507324
Max Magnitude3
ClinVar
Risk rs62507324(C;C)
Alt rs62507324(C;C)
Reference rs62507324(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246590C>G
CLNSRC
CLNACC RCV000089132.1,