| Gene ID:3075 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant |
| Global MAF:A=0.4575/2291 |
| DNA change:c.59-7002G>A |
| Description:complement factor H |
| Chromosome:1:196665976 |
| 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 | |||||||
| T | 0.156 | 0.261 | 0.52 | 0.008 |
| Function:Undone |
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