rs11986414
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11986414(A;A) |
| Make rs11986414(A;G) |
| Make rs11986414(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 1798784 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11986414 |
| dbSNP (classic) | rs11986414 |
| ClinGen | rs11986414 |
| ebi | rs11986414 |
| HLI | rs11986414 |
| Exac | rs11986414 |
| Gnomad | rs11986414 |
| Varsome | rs11986414 |
| LitVar | rs11986414 |
| Map | rs11986414 |
| PheGenI | rs11986414 |
| Biobank | rs11986414 |
| 1000 genomes | rs11986414 |
| hgdp | rs11986414 |
| ensembl | rs11986414 |
| geneview | rs11986414 |
| scholar | rs11986414 |
| rs11986414 | |
| pharmgkb | rs11986414 |
| gwascentral | rs11986414 |
| openSNP | rs11986414 |
| 23andMe | rs11986414 |
| SNPshot | rs11986414 |
| SNPdbe | rs11986414 |
| MSV3d | rs11986414 |
| GWAS Ctlg | rs11986414 |
| GMAF | 0.2677 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 22388998
] Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation
