rs11187870
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs11187870(C;C) |
| Make rs11187870(C;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94328109 |
| Gene | PLCE1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11187870 |
| dbSNP (classic) | rs11187870 |
| ClinGen | rs11187870 |
| ebi | rs11187870 |
| HLI | rs11187870 |
| Exac | rs11187870 |
| Gnomad | rs11187870 |
| Varsome | rs11187870 |
| LitVar | rs11187870 |
| Map | rs11187870 |
| PheGenI | rs11187870 |
| Biobank | rs11187870 |
| 1000 genomes | rs11187870 |
| hgdp | rs11187870 |
| ensembl | rs11187870 |
| geneview | rs11187870 |
| scholar | rs11187870 |
| rs11187870 | |
| pharmgkb | rs11187870 |
| gwascentral | rs11187870 |
| openSNP | rs11187870 |
| 23andMe | rs11187870 |
| SNPshot | rs11187870 |
| SNPdbe | rs11187870 |
| MSV3d | rs11187870 |
| GWAS Ctlg | rs11187870 |
| GMAF | 0.08127 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22203178] Putatively Functional PLCE1 Variants and Susceptibility to Esophageal Squamous Cell Carcinoma (ESCC): A Case-Control Study in Eastern Chinese Populations
[PMID 22412849
] Potentially Functional Variants of PLCE1 Identified by GWASs Contribute to Gastric Adenocarcinoma Susceptibility in an Eastern Chinese Population
[PMID 25992311] Genetic variants and risk of gastric cancer: a pathway analysis of a genome-wide association study
| ClinVar | |
|---|---|
| Risk | rs11187870(C;C) |
| Alt | rs11187870(C;C) |
| Reference | Rs11187870(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | Nephrotic syndrome |
| Variation | info |
| Gene | PLCE1 |
| CLNDBN | Nephrotic syndrome |
| Reversed | 0 |
| HGVS | NC_000010.10:g.96087866G>C |
| CLNSRC | |
| CLNACC | RCV000398900.1, |
