rs606231398
From SNPedia
Merged into | rs80359306 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs606231398(-;A) |
Make rs606231398(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 32333285 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs606231398 |
dbSNP (classic) | rs606231398 |
ClinGen | rs606231398 |
ebi | rs606231398 |
HLI | rs606231398 |
Exac | rs606231398 |
Gnomad | rs606231398 |
Varsome | rs606231398 |
LitVar | rs606231398 |
Map | rs606231398 |
PheGenI | rs606231398 |
Biobank | rs606231398 |
1000 genomes | rs606231398 |
hgdp | rs606231398 |
ensembl | rs606231398 |
geneview | rs606231398 |
scholar | rs606231398 |
rs606231398 | |
pharmgkb | rs606231398 |
gwascentral | rs606231398 |
openSNP | rs606231398 |
23andMe | rs606231398 |
SNPshot | rs606231398 |
SNPdbe | rs606231398 |
MSV3d | rs606231398 |
GWAS Ctlg | rs606231398 |
Status | Merged into rs80359306 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs606231398(A;A) |
Alt | rs606231398(A;A) |
Reference | Rs606231398(;) |
Significance | Pathogenic |
Disease | Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | BRCA2 |
CLNDBN | Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.32907428dupA |
CLNSRC | Breast Cancer Information Core (BRCA2) |
CLNACC | RCV000031343.13, RCV000043897.6, RCV000131453.3, RCV000160269.2, |