rs7097
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs7097(A;A) |
| Make rs7097(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 27623299 |
| Gene | POLR1D |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7097 |
| dbSNP (classic) | rs7097 |
| ClinGen | rs7097 |
| ebi | rs7097 |
| HLI | rs7097 |
| Exac | rs7097 |
| Gnomad | rs7097 |
| Varsome | rs7097 |
| LitVar | rs7097 |
| Map | rs7097 |
| PheGenI | rs7097 |
| Biobank | rs7097 |
| 1000 genomes | rs7097 |
| hgdp | rs7097 |
| ensembl | rs7097 |
| geneview | rs7097 |
| scholar | rs7097 |
| rs7097 | |
| pharmgkb | rs7097 |
| gwascentral | rs7097 |
| openSNP | rs7097 |
| 23andMe | rs7097 |
| SNPshot | rs7097 |
| SNPdbe | rs7097 |
| MSV3d | rs7097 |
| GWAS Ctlg | rs7097 |
| GMAF | 0.3503 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21471979] Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility
| ClinVar | |
|---|---|
| Risk | rs7097(A;A) |
| Alt | rs7097(A;A) |
| Reference | Rs7097(G;G) |
| Significance | Non-pathogenic |
| Disease | Treacher Collins Syndrome |
| Variation | info |
| Gene | POLR1D |
| CLNDBN | Treacher Collins Syndrome, Dominant |
| Reversed | 1 |
| HGVS | NC_000013.10:g.28197436C>T |
| CLNSRC | |
| CLNACC | RCV000273409.1, |
