rs397507765
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;AGTAC) | 6 | BRCA2 variant considered pathogenic for breast cancer |
Make rs397507765(AGTAC;AGTAC) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 32339523 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs397507765 |
dbSNP (classic) | rs397507765 |
ClinGen | rs397507765 |
ebi | rs397507765 |
HLI | rs397507765 |
Exac | rs397507765 |
Gnomad | rs397507765 |
Varsome | rs397507765 |
LitVar | rs397507765 |
Map | rs397507765 |
PheGenI | rs397507765 |
Biobank | rs397507765 |
1000 genomes | rs397507765 |
hgdp | rs397507765 |
ensembl | rs397507765 |
geneview | rs397507765 |
scholar | rs397507765 |
rs397507765 | |
pharmgkb | rs397507765 |
gwascentral | rs397507765 |
openSNP | rs397507765 |
23andMe | rs397507765 |
SNPshot | rs397507765 |
SNPdbe | rs397507765 |
MSV3d | rs397507765 |
GWAS Ctlg | rs397507765 |
Max Magnitude | 6 |
aka c.5164_5168dupAGTAC
ClinVar | |
---|---|
Risk | rs397507765(ACAGT;ACAGT) |
Alt | rs397507765(ACAGT;ACAGT) |
Reference | Rs397507765(-;-) |
Significance | Untested |
Disease | Familial cancer of breast |
Variation | info |
Gene | BRCA2 |
CLNDBN | Familial cancer of breast |
Reversed | 0 |
HGVS | NC_000013.10:g.32913656_32913660dupAGTAC |
CLNSRC | ClinVar |
CLNACC | RCV000044580.2, |