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rs121908629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908629(A;A)
Make rs121908629(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position36236864
GeneGNE
is asnp
is mentioned by
dbSNPrs121908629
ebirs121908629
HLIrs121908629
Exacrs121908629
Varsomers121908629
Maprs121908629
PheGenIrs121908629
hapmaprs121908629
1000 genomesrs121908629
hgdprs121908629
ensemblrs121908629
gopubmedrs121908629
geneviewrs121908629
scholarrs121908629
googlers121908629
pharmgkbrs121908629
gwascentralrs121908629
openSNPrs121908629
23andMers121908629
23andMe allrs121908629
SNP Nexus

SNPshotrs121908629
SNPdbers121908629
MSV3drs121908629
GWAS Ctlgrs121908629
Max Magnitude0
OMIM603824
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908629(A;A)
Alt rs121908629(A;A)
Reference rs121908629(G;G)
Significance Pathogenic
Disease Inclusion body myopathy 2 Nonaka myopathy
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2 Nonaka myopathy
Reversed 1
HGVS NC_000009.11:g.36236861C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006401.5, RCV000202425.1,