Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123392

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123392(A;C)
Make rs398123392(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31861259
GeneNEU1
is asnp
is mentioned by
dbSNPrs398123392
dbSNP (classic)rs398123392
ClinGenrs398123392
ebirs398123392
HLIrs398123392
Exacrs398123392
Gnomadrs398123392
Varsomers398123392
LitVarrs398123392
Maprs398123392
PheGenIrs398123392
Biobankrs398123392
1000 genomesrs398123392
hgdprs398123392
ensemblrs398123392
geneviewrs398123392
scholarrs398123392
googlers398123392
pharmgkbrs398123392
gwascentralrs398123392
openSNPrs398123392
23andMers398123392
23andMe allrs398123392
SNPshotrs398123392
SNPdbers398123392
MSV3drs398123392
GWAS Ctlgrs398123392
Max Magnitude0
ClinVar
Risk rs398123392(C;C) rs398123392(G;G)
Alt rs398123392(C;C) rs398123392(G;G)
Reference Rs398123392(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene NEU1
CLNDBN not provided not specified
Reversed 1
HGVS NC_000006.11:g.31829036T>C; NC_000006.11:g.31829036T>G
CLNSRC
CLNACC RCV000492831.1, RCV000078815.4,