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rs398123577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123577(A;A)
Make rs398123577(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position15694164
GeneNDE1
is asnp
is mentioned by
dbSNPrs398123577
ebirs398123577
HLIrs398123577
Exacrs398123577
Varsomers398123577
Maprs398123577
PheGenIrs398123577
hapmaprs398123577
1000 genomesrs398123577
hgdprs398123577
ensemblrs398123577
gopubmedrs398123577
geneviewrs398123577
scholarrs398123577
googlers398123577
pharmgkbrs398123577
gwascentralrs398123577
openSNPrs398123577
23andMers398123577
23andMe allrs398123577
SNP Nexus

SNPshotrs398123577
SNPdbers398123577
MSV3drs398123577
GWAS Ctlgrs398123577
Max Magnitude0
ClinVar
Risk rs398123577(A;A)
Alt rs398123577(A;A)
Reference Rs398123577(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NDE1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.15788021G>A
CLNSRC ClinVar
CLNACC RCV000079548.4,