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rs377328326

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377328326(A;A)
Make rs377328326(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47945985
GenePNPO
is asnp
is mentioned by
dbSNPrs377328326
ebirs377328326
HLIrs377328326
Exacrs377328326
Varsomers377328326
Maprs377328326
PheGenIrs377328326
hapmaprs377328326
1000 genomesrs377328326
hgdprs377328326
ensemblrs377328326
gopubmedrs377328326
geneviewrs377328326
scholarrs377328326
googlers377328326
pharmgkbrs377328326
gwascentralrs377328326
openSNPrs377328326
23andMers377328326
23andMe allrs377328326
SNP Nexus

SNPshotrs377328326
SNPdbers377328326
MSV3drs377328326
GWAS Ctlgrs377328326
Max Magnitude0
ClinVar
Risk rs377328326(A,T;A,T)
Alt rs377328326(A,T;A,T)
Reference rs377328326(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46023351G>A
CLNSRC
CLNACC RCV000188496.1,