rs17549193
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17549193(C;C) |
| Make rs17549193(C;T) |
| Make rs17549193(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 134887180 |
| Gene | FCN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17549193 |
| dbSNP (classic) | rs17549193 |
| ClinGen | rs17549193 |
| ebi | rs17549193 |
| HLI | rs17549193 |
| Exac | rs17549193 |
| Gnomad | rs17549193 |
| Varsome | rs17549193 |
| LitVar | rs17549193 |
| Map | rs17549193 |
| PheGenI | rs17549193 |
| Biobank | rs17549193 |
| 1000 genomes | rs17549193 |
| hgdp | rs17549193 |
| ensembl | rs17549193 |
| geneview | rs17549193 |
| scholar | rs17549193 |
| rs17549193 | |
| pharmgkb | rs17549193 |
| gwascentral | rs17549193 |
| openSNP | rs17549193 |
| 23andMe | rs17549193 |
| SNPshot | rs17549193 |
| SNPdbe | rs17549193 |
| MSV3d | rs17549193 |
| GWAS Ctlg | rs17549193 |
| GMAF | 0.241 |
| Max Magnitude | 0 |
[PMID 17680820
] Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.
[PMID 19220833] Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.
[PMID 22848725] Mannose-binding lectin deficiency is associated with myocardial infarction: the HUNT2 study in Norway.
[PMID 23525825] Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.
