rs587780033
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587780033(-;A) |
Make rs587780033(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 214781250 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs587780033 |
dbSNP (classic) | rs587780033 |
ClinGen | rs587780033 |
ebi | rs587780033 |
HLI | rs587780033 |
Exac | rs587780033 |
Gnomad | rs587780033 |
Varsome | rs587780033 |
LitVar | rs587780033 |
Map | rs587780033 |
PheGenI | rs587780033 |
Biobank | rs587780033 |
1000 genomes | rs587780033 |
hgdp | rs587780033 |
ensembl | rs587780033 |
geneview | rs587780033 |
scholar | rs587780033 |
rs587780033 | |
pharmgkb | rs587780033 |
gwascentral | rs587780033 |
openSNP | rs587780033 |
23andMe | rs587780033 |
SNPshot | rs587780033 |
SNPdbe | rs587780033 |
MSV3d | rs587780033 |
GWAS Ctlg | rs587780033 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780033(A;A) |
Alt | rs587780033(A;A) |
Reference | Rs587780033(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Familial cancer of breast |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000002.11:g.215645975dupT |
CLNSRC | |
CLNACC | RCV000115638.3, RCV000464884.1, |