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

rs62508734

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a phenylketonuria mutation
Make rs62508734(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852818
GenePAH
is asnp
is mentioned by
dbSNPrs62508734
ebirs62508734
HLIrs62508734
Exacrs62508734
Varsomers62508734
Maprs62508734
PheGenIrs62508734
hapmaprs62508734
1000 genomesrs62508734
hgdprs62508734
ensemblrs62508734
gopubmedrs62508734
geneviewrs62508734
scholarrs62508734
googlers62508734
pharmgkbrs62508734
gwascentralrs62508734
openSNPrs62508734
23andMers62508734
23andMe allrs62508734
SNP Nexus

SNPshotrs62508734
SNPdbers62508734
MSV3drs62508734
GWAS Ctlgrs62508734
Max Magnitude3
ClinVar
Risk rs62508734(G;G)
Alt rs62508734(G;G)
Reference rs62508734(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246596T>C
CLNSRC
CLNACC RCV000089127.1,