rs587780170
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587780170(C;C) |
Make rs587780170(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 28695786 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs587780170 |
dbSNP (classic) | rs587780170 |
ClinGen | rs587780170 |
ebi | rs587780170 |
HLI | rs587780170 |
Exac | rs587780170 |
Gnomad | rs587780170 |
Varsome | rs587780170 |
LitVar | rs587780170 |
Map | rs587780170 |
PheGenI | rs587780170 |
Biobank | rs587780170 |
1000 genomes | rs587780170 |
hgdp | rs587780170 |
ensembl | rs587780170 |
geneview | rs587780170 |
scholar | rs587780170 |
rs587780170 | |
pharmgkb | rs587780170 |
gwascentral | rs587780170 |
openSNP | rs587780170 |
23andMe | rs587780170 |
SNPshot | rs587780170 |
SNPdbe | rs587780170 |
MSV3d | rs587780170 |
GWAS Ctlg | rs587780170 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780170(A;A) rs587780170(C;C) rs587780170(T;T) |
Alt | rs587780170(A;A) rs587780170(C;C) rs587780170(T;T) |
Reference | Rs587780170(G;G) |
Significance | Probable-Pathogenic |
Disease | Neoplasm of breast Hereditary cancer-predisposing syndrome not specified Familial cancer of breast |
Variation | info |
Gene | CHEK2 |
CLNDBN | Neoplasm of breast Hereditary cancer-predisposing syndrome not specified Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000022.10:g.29091774C>A; NC_000022.10:g.29091774C>G; NC_000022.10:g.29091774C>T |
CLNSRC | |
CLNACC | RCV000422650.1, RCV000115987.6, RCV000212454.2, RCV000230538.2, RCV000467802.1, |