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rs121908626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908626(A;A)
Make rs121908626(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position36218225
GeneGNE
is asnp
is mentioned by
dbSNPrs121908626
ebirs121908626
HLIrs121908626
Exacrs121908626
Varsomers121908626
Maprs121908626
PheGenIrs121908626
hapmaprs121908626
1000 genomesrs121908626
hgdprs121908626
ensemblrs121908626
gopubmedrs121908626
geneviewrs121908626
scholarrs121908626
googlers121908626
pharmgkbrs121908626
gwascentralrs121908626
openSNPrs121908626
23andMers121908626
23andMe allrs121908626
SNP Nexus

SNPshotrs121908626
SNPdbers121908626
MSV3drs121908626
GWAS Ctlgrs121908626
Max Magnitude0
OMIM603824
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908626(A;A)
Alt rs121908626(A;A)
Reference rs121908626(G;G)
Significance Pathogenic
Disease Nonaka myopathy
Variation info
Gene GNE
CLNDBN Nonaka myopathy
Reversed 1
HGVS NC_000009.11:g.36218222C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006398.4,