rs730881422
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs730881422(C;T) |
Make rs730881422(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 214730416 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs730881422 |
dbSNP (classic) | rs730881422 |
ClinGen | rs730881422 |
ebi | rs730881422 |
HLI | rs730881422 |
Exac | rs730881422 |
Gnomad | rs730881422 |
Varsome | rs730881422 |
LitVar | rs730881422 |
Map | rs730881422 |
PheGenI | rs730881422 |
Biobank | rs730881422 |
1000 genomes | rs730881422 |
hgdp | rs730881422 |
ensembl | rs730881422 |
geneview | rs730881422 |
scholar | rs730881422 |
rs730881422 | |
pharmgkb | rs730881422 |
gwascentral | rs730881422 |
openSNP | rs730881422 |
23andMe | rs730881422 |
SNPshot | rs730881422 |
SNPdbe | rs730881422 |
MSV3d | rs730881422 |
GWAS Ctlg | rs730881422 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881422(T;T) |
Alt | rs730881422(T;T) |
Reference | Rs730881422(C;C) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome Familial cancer of breast |
Variation | info |
Gene | BARD1 |
CLNDBN | not provided Hereditary cancer-predisposing syndrome Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000002.11:g.215595140G>A |
CLNSRC | |
CLNACC | RCV000159820.2, RCV000222541.1, RCV000225939.2, |