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rs1057517094

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517094(-;A)
Make rs1057517094(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position36236964
GeneGNE
is asnp
is mentioned by
dbSNPrs1057517094
dbSNP (old)rs1057517094
ClinGenrs1057517094
ebirs1057517094
HLIrs1057517094
Exacrs1057517094
Gnomadrs1057517094
Varsomers1057517094
Maprs1057517094
PheGenIrs1057517094
Biobankrs1057517094
1000 genomesrs1057517094
hgdprs1057517094
ensemblrs1057517094
gopubmedrs1057517094
geneviewrs1057517094
scholarrs1057517094
googlers1057517094
pharmgkbrs1057517094
gwascentralrs1057517094
openSNPrs1057517094
23andMers1057517094
23andMe allrs1057517094
SNPshotrs1057517094
SNPdbers1057517094
MSV3drs1057517094
GWAS Ctlgrs1057517094
Max Magnitude0
ClinVar
Risk rs1057517094(A;A)
Alt rs1057517094(A;A)
Reference Rs1057517094(-;-)
Significance Probable-Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 1
HGVS NC_000009.11:g.36236962dupT
CLNSRC
CLNACC RCV000410658.1,