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rs17679445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs17679445(A;A)
Make rs17679445(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position47944699
GenePNPO
is asnp
is mentioned by
dbSNPrs17679445
ebirs17679445
HLIrs17679445
Exacrs17679445
Varsomers17679445
Maprs17679445
PheGenIrs17679445
hapmaprs17679445
1000 genomesrs17679445
hgdprs17679445
ensemblrs17679445
gopubmedrs17679445
geneviewrs17679445
scholarrs17679445
googlers17679445
pharmgkbrs17679445
gwascentralrs17679445
openSNPrs17679445
23andMers17679445
23andMe allrs17679445
SNP Nexus

SNPshotrs17679445
SNPdbers17679445
MSV3drs17679445
GWAS Ctlgrs17679445
GMAF0.03444
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Also known as PNPO Arg116Gln.


GET Evidence
PNPO-R116Q
aa_change Arg116Gln
aa_change_short R116Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.052612
summary



ClinVar
Risk rs17679445(A;A)
Alt rs17679445(A;A)
Reference rs17679445(G;G)
Significance Other
Disease not specified
Variation info
Gene PNPO
CLNDBN not specified
Reversed 0
HGVS NC_000017.10:g.46022065G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000118002.3,