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

rs62507328

From SNPedia

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


Make rs62507328(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855286
GenePAH
is asnp
is mentioned by
dbSNPrs62507328
ebirs62507328
HLIrs62507328
Exacrs62507328
Varsomers62507328
Maprs62507328
PheGenIrs62507328
hapmaprs62507328
1000 genomesrs62507328
hgdprs62507328
ensemblrs62507328
gopubmedrs62507328
geneviewrs62507328
scholarrs62507328
googlers62507328
pharmgkbrs62507328
gwascentralrs62507328
openSNPrs62507328
23andMers62507328
23andMe allrs62507328
SNP Nexus

SNPshotrs62507328
SNPdbers62507328
MSV3drs62507328
GWAS Ctlgrs62507328
Max Magnitude3
ClinVar
Risk rs62507328(;)
Alt rs62507328(;)
Reference rs62507328(A;A)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103249064delT
CLNSRC
CLNACC RCV000088982.1,