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rs121908631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908631(C;T)
Make rs121908631(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position36223405
GeneGNE
is asnp
is mentioned by
dbSNPrs121908631
ebirs121908631
HLIrs121908631
Exacrs121908631
Varsomers121908631
Maprs121908631
PheGenIrs121908631
hapmaprs121908631
1000 genomesrs121908631
hgdprs121908631
ensemblrs121908631
gopubmedrs121908631
geneviewrs121908631
scholarrs121908631
googlers121908631
pharmgkbrs121908631
gwascentralrs121908631
openSNPrs121908631
23andMers121908631
23andMe allrs121908631
SNP Nexus

SNPshotrs121908631
SNPdbers121908631
MSV3drs121908631
GWAS Ctlgrs121908631
Max Magnitude0
OMIM603824
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121908631(T;T)
Alt rs121908631(T;T)
Reference rs121908631(C;C)
Significance Other
Disease Nonaka myopathy
Variation info
Gene GNE
CLNDBN Nonaka myopathy
Reversed 1
HGVS NC_000009.11:g.36223402G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006403.4,