rs1057516657
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GA;GA) | 0 | common in clinvar |
Make rs1057516657(-;-) |
Make rs1057516657(-;GA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 36222866 |
Gene | GNE |
is a | snp |
is | mentioned by |
dbSNP | rs1057516657 |
dbSNP (classic) | rs1057516657 |
ClinGen | rs1057516657 |
ebi | rs1057516657 |
HLI | rs1057516657 |
Exac | rs1057516657 |
Gnomad | rs1057516657 |
Varsome | rs1057516657 |
LitVar | rs1057516657 |
Map | rs1057516657 |
PheGenI | rs1057516657 |
Biobank | rs1057516657 |
1000 genomes | rs1057516657 |
hgdp | rs1057516657 |
ensembl | rs1057516657 |
geneview | rs1057516657 |
scholar | rs1057516657 |
rs1057516657 | |
pharmgkb | rs1057516657 |
gwascentral | rs1057516657 |
openSNP | rs1057516657 |
23andMe | rs1057516657 |
SNPshot | rs1057516657 |
SNPdbe | rs1057516657 |
MSV3d | rs1057516657 |
GWAS Ctlg | rs1057516657 |
Max Magnitude | 0 |
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, |