rs587782245
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587782245(-;-) |
Make rs587782245(-;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 22 |
Position | 28724978 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs587782245 |
dbSNP (classic) | rs587782245 |
ClinGen | rs587782245 |
ebi | rs587782245 |
HLI | rs587782245 |
Exac | rs587782245 |
Gnomad | rs587782245 |
Varsome | rs587782245 |
LitVar | rs587782245 |
Map | rs587782245 |
PheGenI | rs587782245 |
Biobank | rs587782245 |
1000 genomes | rs587782245 |
hgdp | rs587782245 |
ensembl | rs587782245 |
geneview | rs587782245 |
scholar | rs587782245 |
rs587782245 | |
pharmgkb | rs587782245 |
gwascentral | rs587782245 |
openSNP | rs587782245 |
23andMe | rs587782245 |
SNPshot | rs587782245 |
SNPdbe | rs587782245 |
MSV3d | rs587782245 |
GWAS Ctlg | rs587782245 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782245(-;-) |
Alt | rs587782245(-;-) |
Reference | Rs587782245(A;A) |
Significance | Other |
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 | 1 |
HGVS | NC_000022.10:g.29120966delT |
CLNSRC | |
CLNACC | RCV000130949.6, RCV000204563.2, RCV000235159.2, |