rs2151280
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2151280(C;C) |
| Make rs2151280(C;T) |
| Make rs2151280(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 22034720 |
| Gene | CDKN2B-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2151280 |
| dbSNP (classic) | rs2151280 |
| ClinGen | rs2151280 |
| ebi | rs2151280 |
| HLI | rs2151280 |
| Exac | rs2151280 |
| Gnomad | rs2151280 |
| Varsome | rs2151280 |
| LitVar | rs2151280 |
| Map | rs2151280 |
| PheGenI | rs2151280 |
| Biobank | rs2151280 |
| 1000 genomes | rs2151280 |
| hgdp | rs2151280 |
| ensembl | rs2151280 |
| geneview | rs2151280 |
| scholar | rs2151280 |
| rs2151280 | |
| pharmgkb | rs2151280 |
| gwascentral | rs2151280 |
| openSNP | rs2151280 |
| 23andMe | rs2151280 |
| SNPshot | rs2151280 |
| SNPdbe | rs2151280 |
| MSV3d | rs2151280 |
| GWAS Ctlg | rs2151280 |
| GMAF | 0.4734 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe blog rs2151280 G 1.19 Basal Cell Carcinoma
[PMID 19578363
] New common variants affecting susceptibility to basal cell carcinoma
[PMID 22034633] Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1
| GWAS snp | |
|---|---|
| PMID | [PMID 24403052 |
| Trait | Basal cell carcinoma |
| Title | Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. |
| Risk Allele | G |
| P-val | 3E-10 |
| Odds Ratio | 1.20 [1.14-1.27] |
[PMID 25874495] Long noncoding RNAs POLR2E rs3787016 C/T and HULC rs7763881 A/C polymorphisms are associated with decreased risk of esophageal cancer
