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rs769215411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769215411(A;A)
Make rs769215411(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position36246163
GeneGNE
is asnp
is mentioned by
dbSNPrs769215411
dbSNP (classic)rs769215411
ClinGenrs769215411
ebirs769215411
HLIrs769215411
Exacrs769215411
Gnomadrs769215411
Varsomers769215411
LitVarrs769215411
Maprs769215411
PheGenIrs769215411
Biobankrs769215411
1000 genomesrs769215411
hgdprs769215411
ensemblrs769215411
geneviewrs769215411
scholarrs769215411
googlers769215411
pharmgkbrs769215411
gwascentralrs769215411
openSNPrs769215411
23andMers769215411
SNPshotrs769215411
SNPdbers769215411
MSV3drs769215411
GWAS Ctlgrs769215411
Max Magnitude0
ClinVar
Risk rs769215411(A;A)
Alt rs769215411(A;A)
Reference Rs769215411(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GNE
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.36246160G>A
CLNSRC
CLNACC RCV000359295.1,