rs769366055
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs769366055(C;G) |
Make rs769366055(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 43424324 |
Gene | SZT2 |
is a | snp |
is | mentioned by |
dbSNP | rs769366055 |
dbSNP (classic) | rs769366055 |
ClinGen | rs769366055 |
ebi | rs769366055 |
HLI | rs769366055 |
Exac | rs769366055 |
Gnomad | rs769366055 |
Varsome | rs769366055 |
LitVar | rs769366055 |
Map | rs769366055 |
PheGenI | rs769366055 |
Biobank | rs769366055 |
1000 genomes | rs769366055 |
hgdp | rs769366055 |
ensembl | rs769366055 |
geneview | rs769366055 |
scholar | rs769366055 |
rs769366055 | |
pharmgkb | rs769366055 |
gwascentral | rs769366055 |
openSNP | rs769366055 |
23andMe | rs769366055 |
SNPshot | rs769366055 |
SNPdbe | rs769366055 |
MSV3d | rs769366055 |
GWAS Ctlg | rs769366055 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769366055(G;G) |
Alt | rs769366055(G;G) |
Reference | Rs769366055(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SZT2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43889995C>G |
CLNSRC | |
CLNACC | RCV000494105.1, |