rs397507768
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs397507768(G;T) |
Make rs397507768(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 32326499 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs397507768 |
dbSNP (classic) | rs397507768 |
ClinGen | rs397507768 |
ebi | rs397507768 |
HLI | rs397507768 |
Exac | rs397507768 |
Gnomad | rs397507768 |
Varsome | rs397507768 |
LitVar | rs397507768 |
Map | rs397507768 |
PheGenI | rs397507768 |
Biobank | rs397507768 |
1000 genomes | rs397507768 |
hgdp | rs397507768 |
ensembl | rs397507768 |
geneview | rs397507768 |
scholar | rs397507768 |
rs397507768 | |
pharmgkb | rs397507768 |
gwascentral | rs397507768 |
openSNP | rs397507768 |
23andMe | rs397507768 |
SNPshot | rs397507768 |
SNPdbe | rs397507768 |
MSV3d | rs397507768 |
GWAS Ctlg | rs397507768 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397507768(C;C) rs397507768(T;T) |
Alt | rs397507768(C;C) rs397507768(T;T) |
Reference | Rs397507768(G;G) |
Significance | Pathogenic |
Disease | not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Familial cancer of breast |
Variation | info |
Gene | BRCA2 |
CLNDBN | not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Familial cancer of breast |
Reversed | 0 |
HGVS | NC_000013.10:g.32900636G>C; NC_000013.10:g.32900636G>T |
CLNSRC | ClinVar |
CLNACC | RCV000168537.4, RCV000222599.1, RCV000257907.2, RCV000258488.1, RCV000044593.2, RCV000220016.1, RCV000239003.1, |