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rs886042195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position36218201
GeneGNE
is asnp
is mentioned by
dbSNPrs886042195
dbSNP (classic)rs886042195
ClinGenrs886042195
ebirs886042195
HLIrs886042195
Exacrs886042195
Gnomadrs886042195
Varsomers886042195
LitVarrs886042195
Maprs886042195
PheGenIrs886042195
Biobankrs886042195
1000 genomesrs886042195
hgdprs886042195
ensemblrs886042195
geneviewrs886042195
scholarrs886042195
googlers886042195
pharmgkbrs886042195
gwascentralrs886042195
openSNPrs886042195
23andMers886042195
SNPshotrs886042195
SNPdbers886042195
MSV3drs886042195
GWAS Ctlgrs886042195
Max Magnitude0
ClinVar
Risk rs886042195(A;A)
Alt rs886042195(A;A)
Reference Rs886042195(G;G)
Significance Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36218198G>A
CLNSRC
CLNACC RCV000277200.1,