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rs63749677

From SNPedia

Orientationminus
Geno Mag Summary
(-;16) 3 Carrier of a phenylketonuria mutation
(ACCCATTTGGATAAAC;ACCCATTTGGATAAAC) 0 common in clinvar
Make rs63749677(-;-)
Make rs63749677(-;ACCCATTTGGATAAAC)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102894831
GenePAH
is asnp
is mentioned by
dbSNPrs63749677
ebirs63749677
HLIrs63749677
Exacrs63749677
Varsomers63749677
Maprs63749677
PheGenIrs63749677
hapmaprs63749677
1000 genomesrs63749677
hgdprs63749677
ensemblrs63749677
gopubmedrs63749677
geneviewrs63749677
scholarrs63749677
googlers63749677
pharmgkbrs63749677
gwascentralrs63749677
openSNPrs63749677
23andMers63749677
23andMe allrs63749677
SNP Nexus

SNPshotrs63749677
SNPdbers63749677
MSV3drs63749677
GWAS Ctlgrs63749677
Max Magnitude3
ClinVar
Risk rs63749677(;)
Alt rs63749677(;)
Reference rs63749677(ACCCATTTGGATAAAC;ACCCATTTGGATAAAC)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103288609_103288624del16
CLNSRC
CLNACC RCV000088882.1,