rs11037575
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11037575(C;C) |
| Make rs11037575(C;T) |
| Make rs11037575(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 43706780 |
| Gene | HSD17B12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11037575 |
| dbSNP (classic) | rs11037575 |
| ClinGen | rs11037575 |
| ebi | rs11037575 |
| HLI | rs11037575 |
| Exac | rs11037575 |
| Gnomad | rs11037575 |
| Varsome | rs11037575 |
| LitVar | rs11037575 |
| Map | rs11037575 |
| PheGenI | rs11037575 |
| Biobank | rs11037575 |
| 1000 genomes | rs11037575 |
| hgdp | rs11037575 |
| ensembl | rs11037575 |
| geneview | rs11037575 |
| scholar | rs11037575 |
| rs11037575 | |
| pharmgkb | rs11037575 |
| gwascentral | rs11037575 |
| openSNP | rs11037575 |
| 23andMe | rs11037575 |
| SNPshot | rs11037575 |
| SNPdbe | rs11037575 |
| MSV3d | rs11037575 |
| GWAS Ctlg | rs11037575 |
| GMAF | 0.4527 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22941191 ]
|
| Trait | Neuroblastoma |
| Title | Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. |
| Risk Allele | C |
| P-val | 5E-8 |
| Odds Ratio | 1.23 [NR] |
[PMID 18463370] Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.
[PMID 21436895] Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci.
