rs587780021
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587780021(C;T) |
Make rs587780021(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 214745842 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs587780021 |
dbSNP (classic) | rs587780021 |
ClinGen | rs587780021 |
ebi | rs587780021 |
HLI | rs587780021 |
Exac | rs587780021 |
Gnomad | rs587780021 |
Varsome | rs587780021 |
LitVar | rs587780021 |
Map | rs587780021 |
PheGenI | rs587780021 |
Biobank | rs587780021 |
1000 genomes | rs587780021 |
hgdp | rs587780021 |
ensembl | rs587780021 |
geneview | rs587780021 |
scholar | rs587780021 |
rs587780021 | |
pharmgkb | rs587780021 |
gwascentral | rs587780021 |
openSNP | rs587780021 |
23andMe | rs587780021 |
SNPshot | rs587780021 |
SNPdbe | rs587780021 |
MSV3d | rs587780021 |
GWAS Ctlg | rs587780021 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780021(T;T) |
Alt | rs587780021(T;T) |
Reference | Rs587780021(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Familial cancer of breast not provided |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome Familial cancer of breast not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.215610566G>A |
CLNSRC | |
CLNACC | RCV000115616.5, RCV000205536.3, RCV000212135.1, |