rs774175654
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs774175654(-;-) |
Make rs774175654(-;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 22 |
Position | 28689188 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs774175654 |
dbSNP (classic) | rs774175654 |
ClinGen | rs774175654 |
ebi | rs774175654 |
HLI | rs774175654 |
Exac | rs774175654 |
Gnomad | rs774175654 |
Varsome | rs774175654 |
LitVar | rs774175654 |
Map | rs774175654 |
PheGenI | rs774175654 |
Biobank | rs774175654 |
1000 genomes | rs774175654 |
hgdp | rs774175654 |
ensembl | rs774175654 |
geneview | rs774175654 |
scholar | rs774175654 |
rs774175654 | |
pharmgkb | rs774175654 |
gwascentral | rs774175654 |
openSNP | rs774175654 |
23andMe | rs774175654 |
SNPshot | rs774175654 |
SNPdbe | rs774175654 |
MSV3d | rs774175654 |
GWAS Ctlg | rs774175654 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs774175654(-;-) |
Alt | rs774175654(-;-) |
Reference | Rs774175654(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Familial cancer of breast not provided |
Variation | info |
Gene | CHEK2 |
CLNDBN | Hereditary cancer-predisposing syndrome Familial cancer of breast not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.29085176delC |
CLNSRC | |
CLNACC | RCV000164545.1, RCV000226984.1, RCV000482135.1, |