rs587782897
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AT;AT) | 0 | common in clinvar |
Make rs587782897(-;-) |
Make rs587782897(-;AT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 214745152 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs587782897 |
dbSNP (classic) | rs587782897 |
ClinGen | rs587782897 |
ebi | rs587782897 |
HLI | rs587782897 |
Exac | rs587782897 |
Gnomad | rs587782897 |
Varsome | rs587782897 |
LitVar | rs587782897 |
Map | rs587782897 |
PheGenI | rs587782897 |
Biobank | rs587782897 |
1000 genomes | rs587782897 |
hgdp | rs587782897 |
ensembl | rs587782897 |
geneview | rs587782897 |
scholar | rs587782897 |
rs587782897 | |
pharmgkb | rs587782897 |
gwascentral | rs587782897 |
openSNP | rs587782897 |
23andMe | rs587782897 |
SNPshot | rs587782897 |
SNPdbe | rs587782897 |
MSV3d | rs587782897 |
GWAS Ctlg | rs587782897 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782897(-;-) |
Alt | rs587782897(-;-) |
Reference | Rs587782897(AT;AT) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.215609876_215609877delAT |
CLNSRC | |
CLNACC | RCV000132536.3, RCV000414583.1, |