rs431825313
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;AAAA) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(AAAA;AAAA) | 0 | common in clinvar |
Make rs431825313(-;-) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 32338211 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs431825313 |
dbSNP (classic) | rs431825313 |
ClinGen | rs431825313 |
ebi | rs431825313 |
HLI | rs431825313 |
Exac | rs431825313 |
Gnomad | rs431825313 |
Varsome | rs431825313 |
LitVar | rs431825313 |
Map | rs431825313 |
PheGenI | rs431825313 |
Biobank | rs431825313 |
1000 genomes | rs431825313 |
hgdp | rs431825313 |
ensembl | rs431825313 |
geneview | rs431825313 |
scholar | rs431825313 |
rs431825313 | |
pharmgkb | rs431825313 |
gwascentral | rs431825313 |
openSNP | rs431825313 |
23andMe | rs431825313 |
SNPshot | rs431825313 |
SNPdbe | rs431825313 |
MSV3d | rs431825313 |
GWAS Ctlg | rs431825313 |
Merged from | Rs886038097 |
Max Magnitude | 6 |
This appears to be a historic SNP, present in older but not newer versions of dbSNP. It appears to have been replaced by rs80359406.
ClinVar | |
---|---|
Risk | rs431825313(-;-) |
Alt | rs431825313(-;-) |
Reference | Rs431825313(AAAA;AAAA) |
Significance | Pathogenic |
Disease | Breast-ovarian cancer |
Variation | info |
Gene | BRCA2 |
CLNDBN | Breast-ovarian cancer, familial 2 |
Reversed | 0 |
HGVS | NC_000013.10:g.32912349_32912352delAAAA |
CLNSRC | ClinVar |
CLNACC | RCV000241173.2, |