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rs398123281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123281(A;A)
Make rs398123281(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42537517
GeneNAGLU
is asnp
is mentioned by
dbSNPrs398123281
ebirs398123281
HLIrs398123281
Exacrs398123281
Varsomers398123281
Maprs398123281
PheGenIrs398123281
hapmaprs398123281
1000 genomesrs398123281
hgdprs398123281
ensemblrs398123281
gopubmedrs398123281
geneviewrs398123281
scholarrs398123281
googlers398123281
pharmgkbrs398123281
gwascentralrs398123281
openSNPrs398123281
23andMers398123281
23andMe allrs398123281
SNP Nexus

SNPshotrs398123281
SNPdbers398123281
MSV3drs398123281
GWAS Ctlgrs398123281
Max Magnitude0
ClinVar
Risk rs398123281(A;A)
Alt rs398123281(A;A)
Reference rs398123281(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NAGLU
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.40689535G>A
CLNSRC ClinVar Emory University
CLNACC RCV000078459.4,