rs878854909
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6 | Breast cancer associated mutation |
Make rs878854909(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 22 |
Position | 28696924 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs878854909 |
dbSNP (classic) | rs878854909 |
ClinGen | rs878854909 |
ebi | rs878854909 |
HLI | rs878854909 |
Exac | rs878854909 |
Gnomad | rs878854909 |
Varsome | rs878854909 |
LitVar | rs878854909 |
Map | rs878854909 |
PheGenI | rs878854909 |
Biobank | rs878854909 |
1000 genomes | rs878854909 |
hgdp | rs878854909 |
ensembl | rs878854909 |
geneview | rs878854909 |
scholar | rs878854909 |
rs878854909 | |
pharmgkb | rs878854909 |
gwascentral | rs878854909 |
openSNP | rs878854909 |
23andMe | rs878854909 |
SNPshot | rs878854909 |
SNPdbe | rs878854909 |
MSV3d | rs878854909 |
GWAS Ctlg | rs878854909 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs878854909(T;T) |
Alt | rs878854909(T;T) |
Reference | Rs878854909(C;C) |
Significance | Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | CHEK2 |
CLNDBN | Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000022.10:g.29092912G>A |
CLNSRC | |
CLNACC | RCV000229454.1, |