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rs796052870

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052870(C;C)
Make rs796052870(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47941677
GenePNPO, SP2-AS1
is asnp
is mentioned by
dbSNPrs796052870
ebirs796052870
HLIrs796052870
Exacrs796052870
Varsomers796052870
Maprs796052870
PheGenIrs796052870
hapmaprs796052870
1000 genomesrs796052870
hgdprs796052870
ensemblrs796052870
gopubmedrs796052870
geneviewrs796052870
scholarrs796052870
googlers796052870
pharmgkbrs796052870
gwascentralrs796052870
openSNPrs796052870
23andMers796052870
23andMe allrs796052870
SNP Nexus

SNPshotrs796052870
SNPdbers796052870
MSV3drs796052870
GWAS Ctlgrs796052870
Max Magnitude0
ClinVar
Risk rs796052870(C;C)
Alt rs796052870(C;C)
Reference rs796052870(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SP2-AS1 LOC100506325 PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46019043T>C
CLNSRC
CLNACC RCV000188504.1,