rs1135401901
From SNPedia
| Orientation | plus |
| Make rs1135401901(A;A) |
| Make rs1135401901(A;C) |
| Make rs1135401901(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 13 |
| Position | 32338377 |
| Gene | BRCA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1135401901 |
| dbSNP (classic) | rs1135401901 |
| ClinGen | rs1135401901 |
| ebi | rs1135401901 |
| HLI | rs1135401901 |
| Exac | rs1135401901 |
| Gnomad | rs1135401901 |
| Varsome | rs1135401901 |
| LitVar | rs1135401901 |
| Map | rs1135401901 |
| PheGenI | rs1135401901 |
| Biobank | rs1135401901 |
| 1000 genomes | rs1135401901 |
| hgdp | rs1135401901 |
| ensembl | rs1135401901 |
| geneview | rs1135401901 |
| scholar | rs1135401901 |
| rs1135401901 | |
| pharmgkb | rs1135401901 |
| gwascentral | rs1135401901 |
| openSNP | rs1135401901 |
| 23andMe | rs1135401901 |
| SNPshot | rs1135401901 |
| SNPdbe | rs1135401901 |
| MSV3d | rs1135401901 |
| GWAS Ctlg | rs1135401901 |
| Max Magnitude | 0 |
aka NM_000059.3(BRCA2):c.4022C>A or (p.Ser1341Ter)
Pathogenic variant based on expert panel submission to ClinVar
