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rs769765227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769765227(C;T)
Make rs769765227(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31860558
GeneNEU1
is asnp
is mentioned by
dbSNPrs769765227
dbSNP (classic)rs769765227
ClinGenrs769765227
ebirs769765227
HLIrs769765227
Exacrs769765227
Gnomadrs769765227
Varsomers769765227
LitVarrs769765227
Maprs769765227
PheGenIrs769765227
Biobankrs769765227
1000 genomesrs769765227
hgdprs769765227
ensemblrs769765227
geneviewrs769765227
scholarrs769765227
googlers769765227
pharmgkbrs769765227
gwascentralrs769765227
openSNPrs769765227
23andMers769765227
23andMe allrs769765227
SNPshotrs769765227
SNPdbers769765227
MSV3drs769765227
GWAS Ctlgrs769765227
Max Magnitude0
ClinVar
Risk rs769765227(T;T)
Alt rs769765227(T;T)
Reference Rs769765227(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEU1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.31828335C>T
CLNSRC
CLNACC RCV000494284.1,