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rs62514904

From SNPedia

Orientationminus
Make rs62514904(-;-)
Make rs62514904(-;ATC)
Make rs62514904(ATC;ATC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102894802
GenePAH
is asnp
is mentioned by
dbSNPrs62514904
ebirs62514904
HLIrs62514904
Exacrs62514904
Varsomers62514904
Maprs62514904
PheGenIrs62514904
hapmaprs62514904
1000 genomesrs62514904
hgdprs62514904
ensemblrs62514904
gopubmedrs62514904
geneviewrs62514904
scholarrs62514904
googlers62514904
pharmgkbrs62514904
gwascentralrs62514904
openSNPrs62514904
23andMers62514904
23andMe allrs62514904
SNP Nexus

SNPshotrs62514904
SNPdbers62514904
MSV3drs62514904
GWAS Ctlgrs62514904
Max Magnitude
ClinVar
Risk rs62514904(;)
Alt rs62514904(;)
Reference rs62514904(TCA;TCA)
Significance Pathogenic
Disease Phenylketonuria not provided
Variation info
Gene PAH
CLNDBN Phenylketonuria not provided
Reversed 1
HGVS NC_000012.11:g.103288579_103288581delTGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000635.4, RCV000078518.5,