rs1052501
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1052501(A;A) |
| Make rs1052501(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 41883906 |
| Gene | ULK4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1052501 |
| dbSNP (classic) | rs1052501 |
| ClinGen | rs1052501 |
| ebi | rs1052501 |
| HLI | rs1052501 |
| Exac | rs1052501 |
| Gnomad | rs1052501 |
| Varsome | rs1052501 |
| LitVar | rs1052501 |
| Map | rs1052501 |
| PheGenI | rs1052501 |
| Biobank | rs1052501 |
| 1000 genomes | rs1052501 |
| hgdp | rs1052501 |
| ensembl | rs1052501 |
| geneview | rs1052501 |
| scholar | rs1052501 |
| rs1052501 | |
| pharmgkb | rs1052501 |
| gwascentral | rs1052501 |
| openSNP | rs1052501 |
| 23andMe | rs1052501 |
| SNPshot | rs1052501 |
| SNPdbe | rs1052501 |
| MSV3d | rs1052501 |
| GWAS Ctlg | rs1052501 |
| GMAF | 0.2934 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22120009 ]
|
| Trait | |
| Title | Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. |
| Risk Allele | G |
| P-val | 2E-8 |
| Odds Ratio | 1.3200 None |
[PMID 24449210] Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
[PMID 22945773] Single-nucleotide polymorphism rs1052501 associated with monoclonal gammopathy of undetermined significance and multiple myeloma.
| ClinVar | |
|---|---|
| Risk | rs1052501(A;A) |
| Alt | rs1052501(A;A) |
| Reference | Rs1052501(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ULK4 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000003.11:g.41925398C>T |
| CLNSRC | |
| CLNACC | RCV000454745.1, |
