rs876660061
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876660061(-;-) |
Make rs876660061(-;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 214780851 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs876660061 |
dbSNP (classic) | rs876660061 |
ClinGen | rs876660061 |
ebi | rs876660061 |
HLI | rs876660061 |
Exac | rs876660061 |
Gnomad | rs876660061 |
Varsome | rs876660061 |
LitVar | rs876660061 |
Map | rs876660061 |
PheGenI | rs876660061 |
Biobank | rs876660061 |
1000 genomes | rs876660061 |
hgdp | rs876660061 |
ensembl | rs876660061 |
geneview | rs876660061 |
scholar | rs876660061 |
rs876660061 | |
pharmgkb | rs876660061 |
gwascentral | rs876660061 |
openSNP | rs876660061 |
23andMe | rs876660061 |
SNPshot | rs876660061 |
SNPdbe | rs876660061 |
MSV3d | rs876660061 |
GWAS Ctlg | rs876660061 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876660061(-;-) |
Alt | rs876660061(-;-) |
Reference | Rs876660061(G;G) |
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.215645575delC |
CLNSRC | |
CLNACC | RCV000215348.1, RCV000480531.1, |