rs773729410
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs773729410(A;A) |
Make rs773729410(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 36236865 |
Gene | GNE |
is a | snp |
is | mentioned by |
dbSNP | rs773729410 |
dbSNP (classic) | rs773729410 |
ClinGen | rs773729410 |
ebi | rs773729410 |
HLI | rs773729410 |
Exac | rs773729410 |
Gnomad | rs773729410 |
Varsome | rs773729410 |
LitVar | rs773729410 |
Map | rs773729410 |
PheGenI | rs773729410 |
Biobank | rs773729410 |
1000 genomes | rs773729410 |
hgdp | rs773729410 |
ensembl | rs773729410 |
geneview | rs773729410 |
scholar | rs773729410 |
rs773729410 | |
pharmgkb | rs773729410 |
gwascentral | rs773729410 |
openSNP | rs773729410 |
23andMe | rs773729410 |
SNPshot | rs773729410 |
SNPdbe | rs773729410 |
MSV3d | rs773729410 |
GWAS Ctlg | rs773729410 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773729410(A;A) |
Alt | rs773729410(A;A) |
Reference | Rs773729410(G;G) |
Significance | Pathogenic |
Disease | Inclusion body myopathy 2 Sialuria |
Variation | info |
Gene | GNE |
CLNDBN | Inclusion body myopathy 2 Sialuria |
Reversed | 0 |
HGVS | NC_000009.11:g.36236862G>A |
CLNSRC | |
CLNACC | RCV000178150.2, RCV000359773.1, |