| Gene ID:3075 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant |
| Global MAF:G=0.4950/2479 |
| DNA change:c.2237-543G |
| Description:complement factor H |
| Chromosome:1:196727803 |
| Method:PCR | |
|---|---|
| Population:American | Case:Control = 96:736 |
| Related disease:Multifocal choroiditis (MFC) | Year:2008 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| C | 0.277 | 0.472 | 2.2 | <0.001 | |||
| T |
| Function:Undone |
|---|
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