rs137853009
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137853009(A;A) |
Make rs137853009(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 28725030 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs137853009 |
dbSNP (classic) | rs137853009 |
ClinGen | rs137853009 |
ebi | rs137853009 |
HLI | rs137853009 |
Exac | rs137853009 |
Gnomad | rs137853009 |
Varsome | rs137853009 |
LitVar | rs137853009 |
Map | rs137853009 |
PheGenI | rs137853009 |
Biobank | rs137853009 |
1000 genomes | rs137853009 |
hgdp | rs137853009 |
ensembl | rs137853009 |
geneview | rs137853009 |
scholar | rs137853009 |
rs137853009 | |
pharmgkb | rs137853009 |
gwascentral | rs137853009 |
openSNP | rs137853009 |
23andMe | rs137853009 |
SNPshot | rs137853009 |
SNPdbe | rs137853009 |
MSV3d | rs137853009 |
GWAS Ctlg | rs137853009 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853009(A;A) |
Alt | rs137853009(A;A) |
Reference | Rs137853009(G;G) |
Significance | Pathogenic |
Disease | Prostate cancer Hereditary cancer-predisposing syndrome Familial cancer of breast not specified |
Variation | info |
Gene | CHEK2 |
CLNDBN | Prostate cancer, somatic Hereditary cancer-predisposing syndrome Familial cancer of breast not specified |
Reversed | 1 |
HGVS | NC_000022.10:g.29121018C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000005944.5, RCV000116025.7, RCV000206384.2, RCV000212427.2, |