rs769215411
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs769215411(A;A) |
Make rs769215411(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 36246163 |
Gene | GNE |
is a | snp |
is | mentioned by |
dbSNP | rs769215411 |
dbSNP (classic) | rs769215411 |
ClinGen | rs769215411 |
ebi | rs769215411 |
HLI | rs769215411 |
Exac | rs769215411 |
Gnomad | rs769215411 |
Varsome | rs769215411 |
LitVar | rs769215411 |
Map | rs769215411 |
PheGenI | rs769215411 |
Biobank | rs769215411 |
1000 genomes | rs769215411 |
hgdp | rs769215411 |
ensembl | rs769215411 |
geneview | rs769215411 |
scholar | rs769215411 |
rs769215411 | |
pharmgkb | rs769215411 |
gwascentral | rs769215411 |
openSNP | rs769215411 |
23andMe | rs769215411 |
SNPshot | rs769215411 |
SNPdbe | rs769215411 |
MSV3d | rs769215411 |
GWAS Ctlg | rs769215411 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769215411(A;A) |
Alt | rs769215411(A;A) |
Reference | Rs769215411(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GNE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.36246160G>A |
CLNSRC | |
CLNACC | RCV000359295.1, |