rs2989727
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2989727(C;C) |
| Make rs2989727(C;T) |
| Make rs2989727(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 134919852 |
| Gene | FCN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2989727 |
| dbSNP (classic) | rs2989727 |
| ClinGen | rs2989727 |
| ebi | rs2989727 |
| HLI | rs2989727 |
| Exac | rs2989727 |
| Gnomad | rs2989727 |
| Varsome | rs2989727 |
| LitVar | rs2989727 |
| Map | rs2989727 |
| PheGenI | rs2989727 |
| Biobank | rs2989727 |
| 1000 genomes | rs2989727 |
| hgdp | rs2989727 |
| ensembl | rs2989727 |
| geneview | rs2989727 |
| scholar | rs2989727 |
| rs2989727 | |
| pharmgkb | rs2989727 |
| gwascentral | rs2989727 |
| openSNP | rs2989727 |
| 23andMe | rs2989727 |
| SNPshot | rs2989727 |
| SNPdbe | rs2989727 |
| MSV3d | rs2989727 |
| GWAS Ctlg | rs2989727 |
| GMAF | 0.478 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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[PMID 18032536] the A allele rs2989727 was significantly increased in RA patients (67%) compared with controls (60%) (P = 0.002). Also, the frequency of the G allele of rs1071583 was increased in RA patients (68%) compared with controls (61%) (P = 0.003).
[PMID 22940091] Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients.
[PMID 22941510] Susceptibility to leprosy is associated with M-ficolin polymorphisms.
