rs1064792962
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAAGCA;CAAGCA) | 0 | common in clinvar |
Chromosome | 13 |
Position | 32354968 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs1064792962 |
dbSNP (classic) | rs1064792962 |
ClinGen | rs1064792962 |
ebi | rs1064792962 |
HLI | rs1064792962 |
Exac | rs1064792962 |
Gnomad | rs1064792962 |
Varsome | rs1064792962 |
LitVar | rs1064792962 |
Map | rs1064792962 |
PheGenI | rs1064792962 |
Biobank | rs1064792962 |
1000 genomes | rs1064792962 |
hgdp | rs1064792962 |
ensembl | rs1064792962 |
geneview | rs1064792962 |
scholar | rs1064792962 |
rs1064792962 | |
pharmgkb | rs1064792962 |
gwascentral | rs1064792962 |
openSNP | rs1064792962 |
23andMe | rs1064792962 |
SNPshot | rs1064792962 |
SNPdbe | rs1064792962 |
MSV3d | rs1064792962 |
GWAS Ctlg | rs1064792962 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064792962(GC;GC) |
Alt | rs1064792962(GC;GC) |
Reference | Rs1064792962(CAAGCA;CAAGCA) |
Significance | Pathogenic |
Disease | Hereditary breast and ovarian cancer syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | Hereditary breast and ovarian cancer syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32929105_32929110delCAAGCAinsGC |
CLNSRC | |
CLNACC | RCV000465804.1, |