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rs139425890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs139425890(A;A)
Make rs139425890(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position36246120
GeneGNE
is asnp
is mentioned by
dbSNPrs139425890
ebirs139425890
HLIrs139425890
Exacrs139425890
Varsomers139425890
Maprs139425890
PheGenIrs139425890
hapmaprs139425890
1000 genomesrs139425890
hgdprs139425890
ensemblrs139425890
gopubmedrs139425890
geneviewrs139425890
scholarrs139425890
googlers139425890
pharmgkbrs139425890
gwascentralrs139425890
openSNPrs139425890
23andMers139425890
23andMe allrs139425890
SNP Nexus

SNPshotrs139425890
SNPdbers139425890
MSV3drs139425890
GWAS Ctlgrs139425890
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs139425890(A;A)
Alt rs139425890(A;A)
Reference rs139425890(T;T)
Significance Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36246117T>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034132.3,