rs786201868
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Make rs786201868(-;-) |
Make rs786201868(-;AG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 214781013 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs786201868 |
dbSNP (classic) | rs786201868 |
ClinGen | rs786201868 |
ebi | rs786201868 |
HLI | rs786201868 |
Exac | rs786201868 |
Gnomad | rs786201868 |
Varsome | rs786201868 |
LitVar | rs786201868 |
Map | rs786201868 |
PheGenI | rs786201868 |
Biobank | rs786201868 |
1000 genomes | rs786201868 |
hgdp | rs786201868 |
ensembl | rs786201868 |
geneview | rs786201868 |
scholar | rs786201868 |
rs786201868 | |
pharmgkb | rs786201868 |
gwascentral | rs786201868 |
openSNP | rs786201868 |
23andMe | rs786201868 |
SNPshot | rs786201868 |
SNPdbe | rs786201868 |
MSV3d | rs786201868 |
GWAS Ctlg | rs786201868 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201868(-;-) |
Alt | rs786201868(-;-) |
Reference | Rs786201868(AG;AG) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000002.11:g.215645737_215645738delCT |
CLNSRC | |
CLNACC | RCV000164367.1, |