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rs62642920

From SNPedia

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


Make rs62642920(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102851695
GenePAH
is asnp
is mentioned by
dbSNPrs62642920
ebirs62642920
HLIrs62642920
Exacrs62642920
Varsomers62642920
Maprs62642920
PheGenIrs62642920
hapmaprs62642920
1000 genomesrs62642920
hgdprs62642920
ensemblrs62642920
gopubmedrs62642920
geneviewrs62642920
scholarrs62642920
googlers62642920
pharmgkbrs62642920
gwascentralrs62642920
openSNPrs62642920
23andMers62642920
23andMe allrs62642920
SNP Nexus

SNPshotrs62642920
SNPdbers62642920
MSV3drs62642920
GWAS Ctlgrs62642920
Max Magnitude3
ClinVar
Risk rs62642920(;)
Alt rs62642920(;)
Reference rs62642920(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103245473delA
CLNSRC
CLNACC RCV000089150.1,