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rs372872777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372872777(A;A)
Make rs372872777(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position36246262
GeneGNE
is asnp
is mentioned by
dbSNPrs372872777
dbSNP (classic)rs372872777
ClinGenrs372872777
ebirs372872777
HLIrs372872777
Exacrs372872777
Gnomadrs372872777
Varsomers372872777
LitVarrs372872777
Maprs372872777
PheGenIrs372872777
Biobankrs372872777
1000 genomesrs372872777
hgdprs372872777
ensemblrs372872777
geneviewrs372872777
scholarrs372872777
googlers372872777
pharmgkbrs372872777
gwascentralrs372872777
openSNPrs372872777
23andMers372872777
SNPshotrs372872777
SNPdbers372872777
MSV3drs372872777
GWAS Ctlgrs372872777
Max Magnitude0
ClinVar
Risk rs372872777(A;A)
Alt rs372872777(A;A)
Reference Rs372872777(G;G)
Significance Probable-Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36246259G>A
CLNSRC
CLNACC RCV000411076.1,