rs157935
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs157935(G;G) |
| Make rs157935(G;T) |
| Make rs157935(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 130900794 |
| Gene | LINC-PINT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs157935 |
| dbSNP (classic) | rs157935 |
| ClinGen | rs157935 |
| ebi | rs157935 |
| HLI | rs157935 |
| Exac | rs157935 |
| Gnomad | rs157935 |
| Varsome | rs157935 |
| LitVar | rs157935 |
| Map | rs157935 |
| PheGenI | rs157935 |
| Biobank | rs157935 |
| 1000 genomes | rs157935 |
| hgdp | rs157935 |
| ensembl | rs157935 |
| geneview | rs157935 |
| scholar | rs157935 |
| rs157935 | |
| pharmgkb | rs157935 |
| gwascentral | rs157935 |
| openSNP | rs157935 |
| 23andMe | rs157935 |
| SNPshot | rs157935 |
| SNPdbe | rs157935 |
| MSV3d | rs157935 |
| GWAS Ctlg | rs157935 |
| GMAF | 0.3301 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe blog rs157935 T 1.23 Basal Cell Carcinoma parental imprinting effect
[PMID 19578363
] New common variants affecting susceptibility to basal cell carcinoma
| 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 | T |
| P-val | 9E-11 |
| Odds Ratio | 1.23 [1.15-1.31] |
