rs2070833
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2070833(A;A) |
Make rs2070833(A;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 43090832 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs2070833 |
dbSNP (classic) | rs2070833 |
ClinGen | rs2070833 |
ebi | rs2070833 |
HLI | rs2070833 |
Exac | rs2070833 |
Gnomad | rs2070833 |
Varsome | rs2070833 |
LitVar | rs2070833 |
Map | rs2070833 |
PheGenI | rs2070833 |
Biobank | rs2070833 |
1000 genomes | rs2070833 |
hgdp | rs2070833 |
ensembl | rs2070833 |
geneview | rs2070833 |
scholar | rs2070833 |
rs2070833 | |
pharmgkb | rs2070833 |
gwascentral | rs2070833 |
openSNP | rs2070833 |
23andMe | rs2070833 |
SNPshot | rs2070833 |
SNPdbe | rs2070833 |
MSV3d | rs2070833 |
GWAS Ctlg | rs2070833 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 25463638] Association of genetic polymorphisms in AURKA, BRCA1, CCNE1 and CDK2 with the risk of endometrial carcinoma and clinicopathological parameters among Chinese Han women
ClinVar | |
---|---|
Risk | rs2070833(A;A) |
Alt | rs2070833(A;A) |
Reference | Rs2070833(C;C) |
Significance | Non-pathogenic |
Disease | Breast-ovarian cancer |
Variation | info |
Gene | BRCA1 |
CLNDBN | Breast-ovarian cancer, familial 1 |
Reversed | 1 |
HGVS | NC_000017.10:g.41242849G>T |
CLNSRC | |
CLNACC | RCV000191388.1, |