rs587782504
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AT;AT) | 0 | common in clinvar |
Make rs587782504(-;-) |
Make rs587782504(-;AT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 214730479 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs587782504 |
dbSNP (classic) | rs587782504 |
ClinGen | rs587782504 |
ebi | rs587782504 |
HLI | rs587782504 |
Exac | rs587782504 |
Gnomad | rs587782504 |
Varsome | rs587782504 |
LitVar | rs587782504 |
Map | rs587782504 |
PheGenI | rs587782504 |
Biobank | rs587782504 |
1000 genomes | rs587782504 |
hgdp | rs587782504 |
ensembl | rs587782504 |
geneview | rs587782504 |
scholar | rs587782504 |
rs587782504 | |
pharmgkb | rs587782504 |
gwascentral | rs587782504 |
openSNP | rs587782504 |
23andMe | rs587782504 |
SNPshot | rs587782504 |
SNPdbe | rs587782504 |
MSV3d | rs587782504 |
GWAS Ctlg | rs587782504 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782504(-;-) |
Alt | rs587782504(-;-) |
Reference | Rs587782504(AT;AT) |
Significance | Other |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000002.11:g.215595203_215595204delAT |
CLNSRC | |
CLNACC | RCV000131644.3, |