rs8176199
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs8176199(A;C) |
Make rs8176199(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 43078507 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs8176199 |
dbSNP (classic) | rs8176199 |
ClinGen | rs8176199 |
ebi | rs8176199 |
HLI | rs8176199 |
Exac | rs8176199 |
Gnomad | rs8176199 |
Varsome | rs8176199 |
LitVar | rs8176199 |
Map | rs8176199 |
PheGenI | rs8176199 |
Biobank | rs8176199 |
1000 genomes | rs8176199 |
hgdp | rs8176199 |
ensembl | rs8176199 |
geneview | rs8176199 |
scholar | rs8176199 |
rs8176199 | |
pharmgkb | rs8176199 |
gwascentral | rs8176199 |
openSNP | rs8176199 |
23andMe | rs8176199 |
SNPshot | rs8176199 |
SNPdbe | rs8176199 |
MSV3d | rs8176199 |
GWAS Ctlg | rs8176199 |
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 | rs8176199(C;C) |
Alt | rs8176199(C;C) |
Reference | Rs8176199(A;A) |
Significance | Non-pathogenic |
Disease | Breast-ovarian cancer |
Variation | info |
Gene | BRCA1 |
CLNDBN | Breast-ovarian cancer, familial 1 |
Reversed | 1 |
HGVS | NC_000017.10:g.41230524T>G |
CLNSRC | |
CLNACC | RCV000191337.1, |