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rs769266169

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769266169(C;T)
Make rs769266169(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47946669
GenePNPO
is asnp
is mentioned by
dbSNPrs769266169
ebirs769266169
HLIrs769266169
Exacrs769266169
Varsomers769266169
Maprs769266169
PheGenIrs769266169
hapmaprs769266169
1000 genomesrs769266169
hgdprs769266169
ensemblrs769266169
gopubmedrs769266169
geneviewrs769266169
scholarrs769266169
googlers769266169
pharmgkbrs769266169
gwascentralrs769266169
openSNPrs769266169
23andMers769266169
23andMe allrs769266169
SNP Nexus

SNPshotrs769266169
SNPdbers769266169
MSV3drs769266169
GWAS Ctlgrs769266169
Max Magnitude0
ClinVar
Risk rs769266169(T;T)
Alt rs769266169(T;T)
Reference rs769266169(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46024035C>T
CLNSRC
CLNACC RCV000188498.2,