rs4151659
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs4151659(A;G) |
| Make rs4151659(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31950687 |
| Gene | CFB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4151659 |
| dbSNP (classic) | rs4151659 |
| ClinGen | rs4151659 |
| ebi | rs4151659 |
| HLI | rs4151659 |
| Exac | rs4151659 |
| Gnomad | rs4151659 |
| Varsome | rs4151659 |
| LitVar | rs4151659 |
| Map | rs4151659 |
| PheGenI | rs4151659 |
| Biobank | rs4151659 |
| 1000 genomes | rs4151659 |
| hgdp | rs4151659 |
| ensembl | rs4151659 |
| geneview | rs4151659 |
| scholar | rs4151659 |
| rs4151659 | |
| pharmgkb | rs4151659 |
| gwascentral | rs4151659 |
| openSNP | rs4151659 |
| 23andMe | rs4151659 |
| SNPshot | rs4151659 |
| SNPdbe | rs4151659 |
| MSV3d | rs4151659 |
| GWAS Ctlg | rs4151659 |
| GMAF | 0.01837 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20054343
] Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes
[PMID 18806293] Analysis of rare variants in the complement component 2 (C2) and factor B (BF) genes refine association for age-related macular degeneration (AMD).
[PMID 19143814] Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1.
[PMID 19143815] MHC fine mapping of human type 1 diabetes using the T1DGC data.
[PMID 19259132] Multilocus analysis of age-related macular degeneration.
| ClinVar | |
|---|---|
| Risk | rs4151659(G;G) |
| Alt | rs4151659(G;G) |
| Reference | Rs4151659(A;A) |
| Significance | Probable-non-pathogenic |
| Disease | Atypical hemolytic uremic syndrome Macular degeneration |
| Variation | info |
| Gene | CFB |
| CLNDBN | Atypical hemolytic uremic syndrome Macular degeneration |
| Reversed | 0 |
| HGVS | NC_000006.11:g.31918464A>G |
| CLNSRC | |
| CLNACC | RCV000272181.1, RCV000364523.1, |
