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rs148597698

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148597698(A;A)
Make rs148597698(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position47945914
GenePNPO
is asnp
is mentioned by
dbSNPrs148597698
ebirs148597698
HLIrs148597698
Exacrs148597698
Varsomers148597698
Maprs148597698
PheGenIrs148597698
hapmaprs148597698
1000 genomesrs148597698
hgdprs148597698
ensemblrs148597698
gopubmedrs148597698
geneviewrs148597698
scholarrs148597698
googlers148597698
pharmgkbrs148597698
gwascentralrs148597698
openSNPrs148597698
23andMers148597698
23andMe allrs148597698
SNP Nexus

SNPshotrs148597698
SNPdbers148597698
MSV3drs148597698
GWAS Ctlgrs148597698
Max Magnitude0
ClinVar
Risk rs148597698(A;A)
Alt rs148597698(A;A)
Reference rs148597698(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PNPO
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.46023280C>A
CLNSRC
CLNACC RCV000188490.1,