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rs886044449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position36219968
GeneGNE
is asnp
is mentioned by
dbSNPrs886044449
dbSNP (classic)rs886044449
ClinGenrs886044449
ebirs886044449
HLIrs886044449
Exacrs886044449
Gnomadrs886044449
Varsomers886044449
LitVarrs886044449
Maprs886044449
PheGenIrs886044449
Biobankrs886044449
1000 genomesrs886044449
hgdprs886044449
ensemblrs886044449
geneviewrs886044449
scholarrs886044449
googlers886044449
pharmgkbrs886044449
gwascentralrs886044449
openSNPrs886044449
23andMers886044449
SNPshotrs886044449
SNPdbers886044449
MSV3drs886044449
GWAS Ctlgrs886044449
Max Magnitude0
ClinVar
Risk rs886044449(-;-)
Alt rs886044449(-;-)
Reference Rs886044449(G;G)
Significance Other
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 0
HGVS NC_000009.11:g.36219965delG
CLNSRC
CLNACC RCV000280041.1,