rs11085735
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11085735(A;A) |
| Make rs11085735(A;C) |
| Make rs11085735(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 10491504 |
| Gene | KEAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11085735 |
| dbSNP (classic) | rs11085735 |
| ClinGen | rs11085735 |
| ebi | rs11085735 |
| HLI | rs11085735 |
| Exac | rs11085735 |
| Gnomad | rs11085735 |
| Varsome | rs11085735 |
| LitVar | rs11085735 |
| Map | rs11085735 |
| PheGenI | rs11085735 |
| Biobank | rs11085735 |
| 1000 genomes | rs11085735 |
| hgdp | rs11085735 |
| ensembl | rs11085735 |
| geneview | rs11085735 |
| scholar | rs11085735 |
| rs11085735 | |
| pharmgkb | rs11085735 |
| gwascentral | rs11085735 |
| openSNP | rs11085735 |
| 23andMe | rs11085735 |
| SNPshot | rs11085735 |
| SNPdbe | rs11085735 |
| MSV3d | rs11085735 |
| GWAS Ctlg | rs11085735 |
| GMAF | 0.06841 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
[PMID 22693272
] NFE2L2 pathway polymorphisms and lung function decline in chronic obstructive pulmonary disease
[PMID 19671143] Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population.
[PMID 20196834] Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.
