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rs62642910

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Carrier of a phenylketonuria mutation
Make rs62642910(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102851715
GenePAH
is asnp
is mentioned by
dbSNPrs62642910
ebirs62642910
HLIrs62642910
Exacrs62642910
Varsomers62642910
Maprs62642910
PheGenIrs62642910
hapmaprs62642910
1000 genomesrs62642910
hgdprs62642910
ensemblrs62642910
gopubmedrs62642910
geneviewrs62642910
scholarrs62642910
googlers62642910
pharmgkbrs62642910
gwascentralrs62642910
openSNPrs62642910
23andMers62642910
23andMe allrs62642910
SNP Nexus

SNPshotrs62642910
SNPdbers62642910
MSV3drs62642910
GWAS Ctlgrs62642910
Max Magnitude3
ClinVar
Risk rs62642910(G;G)
Alt rs62642910(G;G)
Reference rs62642910(C;C)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103245493G>C
CLNSRC
CLNACC RCV000089145.1,