Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057516657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1057516657(-;-)
Make rs1057516657(-;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position36222866
GeneGNE
is asnp
is mentioned by
dbSNPrs1057516657
dbSNP (old)rs1057516657
ClinGenrs1057516657
ebirs1057516657
HLIrs1057516657
Exacrs1057516657
Gnomadrs1057516657
Varsomers1057516657
Maprs1057516657
PheGenIrs1057516657
Biobankrs1057516657
1000 genomesrs1057516657
hgdprs1057516657
ensemblrs1057516657
gopubmedrs1057516657
geneviewrs1057516657
scholarrs1057516657
googlers1057516657
pharmgkbrs1057516657
gwascentralrs1057516657
openSNPrs1057516657
23andMers1057516657
23andMe allrs1057516657
SNPshotrs1057516657
SNPdbers1057516657
MSV3drs1057516657
GWAS Ctlgrs1057516657
Max Magnitude0
ClinVar
Risk rs1057516657(-;-)
Alt rs1057516657(-;-)
Reference Rs1057516657(GA;GA)
Significance Probable-Pathogenic
Disease Inclusion body myopathy 2
Variation info
Gene GNE
CLNDBN Inclusion body myopathy 2
Reversed 1
HGVS NC_000009.11:g.36222863_36222864delTC
CLNSRC
CLNACC RCV000411921.1,