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rs796052869

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052869(A;T)
Make rs796052869(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47946321
GenePNPO
is asnp
is mentioned by
dbSNPrs796052869
ebirs796052869
HLIrs796052869
Exacrs796052869
Varsomers796052869
Maprs796052869
PheGenIrs796052869
hapmaprs796052869
1000 genomesrs796052869
hgdprs796052869
ensemblrs796052869
gopubmedrs796052869
geneviewrs796052869
scholarrs796052869
googlers796052869
pharmgkbrs796052869
gwascentralrs796052869
openSNPrs796052869
23andMers796052869
23andMe allrs796052869
SNP Nexus

SNPshotrs796052869
SNPdbers796052869
MSV3drs796052869
GWAS Ctlgrs796052869
Max Magnitude0
ClinVar
Risk rs796052869(T;T)
Alt rs796052869(T;T)
Reference rs796052869(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46023687A>T
CLNSRC
CLNACC RCV000188497.1,