rs377153250
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs377153250(C;C) |
| Make rs377153250(C;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 2 |
| Position | 214780658 |
| Gene | BARD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs377153250 |
| dbSNP (classic) | rs377153250 |
| ClinGen | rs377153250 |
| ebi | rs377153250 |
| HLI | rs377153250 |
| Exac | rs377153250 |
| Gnomad | rs377153250 |
| Varsome | rs377153250 |
| LitVar | rs377153250 |
| Map | rs377153250 |
| PheGenI | rs377153250 |
| Biobank | rs377153250 |
| 1000 genomes | rs377153250 |
| hgdp | rs377153250 |
| ensembl | rs377153250 |
| geneview | rs377153250 |
| scholar | rs377153250 |
| rs377153250 | |
| pharmgkb | rs377153250 |
| gwascentral | rs377153250 |
| openSNP | rs377153250 |
| 23andMe | rs377153250 |
| SNPshot | rs377153250 |
| SNPdbe | rs377153250 |
| MSV3d | rs377153250 |
| GWAS Ctlg | rs377153250 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs377153250(A;A) rs377153250(C;C) |
| Alt | rs377153250(A;A) rs377153250(C;C) |
| Reference | Rs377153250(G;G) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome not specified |
| Variation | info |
| Gene | BARD1 |
| CLNDBN | Hereditary cancer-predisposing syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000002.11:g.215645382G>A; NC_000002.11:g.215645382G>C |
| CLNSRC | |
| CLNACC | RCV000217217.1, RCV000130569.5, RCV000212125.1, |
