rs876660541
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;TTTT) | 6 | BRCA2 variant considered pathogenic for breast cancer |
Make rs876660541(TTTT;TTTT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 13 |
Position | 32341057 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs876660541 |
dbSNP (classic) | rs876660541 |
ClinGen | rs876660541 |
ebi | rs876660541 |
HLI | rs876660541 |
Exac | rs876660541 |
Gnomad | rs876660541 |
Varsome | rs876660541 |
LitVar | rs876660541 |
Map | rs876660541 |
PheGenI | rs876660541 |
Biobank | rs876660541 |
1000 genomes | rs876660541 |
hgdp | rs876660541 |
ensembl | rs876660541 |
geneview | rs876660541 |
scholar | rs876660541 |
rs876660541 | |
pharmgkb | rs876660541 |
gwascentral | rs876660541 |
openSNP | rs876660541 |
23andMe | rs876660541 |
SNPshot | rs876660541 |
SNPdbe | rs876660541 |
MSV3d | rs876660541 |
GWAS Ctlg | rs876660541 |
Max Magnitude | 6 |
aka c.6699_6702dupTTTT; however, rs876660541 has been merged into rs587781516
ClinVar | |
---|---|
Risk | rs876660541(TTTT;TTTT) |
Alt | rs876660541(TTTT;TTTT) |
Reference | Rs876660541(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRCA2 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000013.10:g.32915191_32915194dupTTTT |
CLNSRC | |
CLNACC | RCV000215061.1, |