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

rs62514929

From SNPedia

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


Make rs62514929(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855210
GenePAH
is asnp
is mentioned by
dbSNPrs62514929
ebirs62514929
HLIrs62514929
Exacrs62514929
Varsomers62514929
Maprs62514929
PheGenIrs62514929
hapmaprs62514929
1000 genomesrs62514929
hgdprs62514929
ensemblrs62514929
gopubmedrs62514929
geneviewrs62514929
scholarrs62514929
googlers62514929
pharmgkbrs62514929
gwascentralrs62514929
openSNPrs62514929
23andMers62514929
23andMe allrs62514929
SNP Nexus

SNPshotrs62514929
SNPdbers62514929
MSV3drs62514929
GWAS Ctlgrs62514929
Max Magnitude3
ClinVar
Risk rs62514929(;)
Alt rs62514929(;)
Reference rs62514929(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103248988delG
CLNSRC
CLNACC RCV000089017.1,